Abstract
Construction of C-N bond continues to be one part of the most significant goals in organic chemistry because of the universal applications of amines in pharmaceuticals, materials and agrochemicals. However, E2 elimination through classic SN2 substitution of alkyl halides lead to generation of alkenes as major side-products. Thus, formation of a challenging C(sp3)-N bond especially on tertiary carbon center remains highly desirable. Herein, we present a practical alternative to prepare primary, secondary and tertiary alkyl amines with high efficiency between alkyl iodides and easily accessible diazonium salts. This robust transformation only employs Cs2CO3 promoting halogen-atom transfer (XAT) process under transition-metal-free reaction conditions, thus providing a rapid method to assemble diverse C(sp3)-N bonds. Moreover, diazonium salts served as alkyl radical initiator and amination reagent in the reaction. Mechanism studies suggest this reaction undergo through halogen-atom transfer process to generate active alkyl radical which couples with diazonium cations to furnish final products.
Similar content being viewed by others
Introduction
Carbon radical has been well recognized as an easily-generated, reactive, and variable species in organic synthesis1. As a result, the design of reaction via radical process provides numerous opportunities to address the shortcomings in ionic chemistry1. For example, homolytic cleavage of C-halogen bonds of alkyl halide makes it possible for the generation of alkyl radical, which can be further functionalized to access highly valuable alkyl substituted products (Fig. 1a)2. However, this strategy usually requires specialized lights with high-energy and the reaction is always found to be with poor functional group tolerance2,3,4. More recently, two main approaches including excited metal catalysis (amido–Cu(I) complex)5,6,7,8,9,10 or metallaphotoredox catlysis11,12,13 combined with UV or visible light which were mainly developed by MacMillan, Fu, and Peters groups have been well-established with high efficiency (Fig. 1a, up). In particular, high-energy UV-light irradiation (hν = 254 nm) is utilized to promote the reaction largely depend on the matching of reduction potentials from different substrates (Ered < −2 V vs saturated calomel electrode for unactivated alkyl iodides)2,3,14.
a Comparation of homolysis of C-halogen bond, SET (single electron transfer), and XAT (halogen-atom transfer) for the formation of alkyl carbon radical. b Classic method for the construction of C–N bonds via SN2 substitutions. c Our reaction design: base-induced XAT (halogen-atom transfer) process of primary, secondary, and tertiary alkyl iodides and diazonium salts act as two critical roles in the amination of corresponding substrates.
Halogen-atom transfer (XAT), which much differs from the above two strategies, provides promising avenues for diverse functionalizations based on the bond dissociation energy (BDE) and the polarizability of the C-halogen bond (Fig. 1a, down)1,15,16. To trigger the homolytic activation of organic halides through XAT process, various abstractors such as α-aminoalkyl radicals, catalytic Mn specie, organosiliane, and Tin have been developed recently due to the weak C-halogen energy (50–70 kcal/mol for C–I bond)1,17. Leonori17,18,19,20,21 and Doyle groups22,23 independently disclosed α-aminoalkyl radicals could abstract the iodide atom under very mild reaction conditions to generate the active alkyl radical which would couple efficiently with broad nucleophiles to construct C–C, C–N, and C–S bonds. Manganese also exhibited powerful reactivity in converting alkyl iodides to alkyl radicals, producing a series of valuable compounds in high yields24,25. Very recently, Liu successfully achieved the copper-catalyzed difluoromethylation of alkyl iodides with high efficiency via halogen abstraction of C–I bonds by aryl radical from aryl diazonium salts, demonstrating the synthetic applicability of this powerful strategy26. Aliphatic amines have been recognized as one of the most privileged scaffolds in pharmaceuticals, agrochemicals, and organic chemistry due to their unique physical, chemical, and biological properties27,28. Consequently, it will be of great value to synthesize structure-varied mines, especially bearing a tertiary carbon atom and their derivatives which has become a long-standing goal for the chemists29,30,31,32,33,34,35,36,37,38. Classical SN2 amination of corresponding alkyl halides with nitrogen nucleophiles across the chemical industries represents a straightforward method to construct alkyl amines (Fig. 1b). However, this process is only limited to the primary substrate due to the less steric hindrance (~93% successful cases). In contrast, secondary (only ~6% successful cases) and tertiary (only ~1% successful cases) substrates are seriously difficult to process the displacement, and alkenes are obtained as the major side products through competitive E2-elimination20,39. Azo-compounds have been found as a kind of critical compounds which could be applied in numerous areas such as dyes40, photoswitches41, and pharmaceuticals42. Consequently, precise and efficient methods to access C–N bonds, especially on secondary or tertiary carbon atom centers through suitable pathways such as the radical process are much more problematic and challenging.
Dual role synthetic system of one compound has been widely applied in organic reactions by avoiding using of additional reagents, simplifying the operation, and improving the efficiency of the transformation43,44,45,46. Readily available diazonium salts have been recognized as versatile building blocks in organic synthesis because they are conveniently synthesized from the corresponding anilines and can undergo radical or electrophilic reaction pathways47,48,49,50,51,52,53,54,55,56. Moreover, the generation of aryl radical from diazonium salts requires additional equipment or technology such as thermal, photochemical, and electrochemical systems56,57,58,59,60. Kinetically favorable XAT occurs to deliver the aryl iodide (rate constant k = 109M−1 s−1), resulting in the formation of more stable alkyl radicals (Fig. 1c, right)24. Inspired by the pioneering work on the iodine atom abstraction from the silyl methyl iodide moiety by Gevorgyan61, we envisioned whether diazonium salts could serve as both “radical abstractor” from alkyl halides for the formation of alkyl radical via XAT process and nitrogen source which can undergo coupling with the “in-situ” alkyl radical to assemble diverse C(sp3)-N bonds (Fig. 1c, left).
In this work, we developed an efficient method via XAT process in presence of base to construct a series of unsymmetric arylalkyldiazenes from alkyl iodides and diazonium salts. To achieve the proposed transformation, a suitable base is essential to promote the formation of aryl radical from diazonium salts, while additional reductants were required to promote the SET process from diazonium salts to generate the aryl radical in the previous reports47,62,63,64. Compared to primary alkyl radical, the tertiary carbon-centered radical was considered as more reactive toward the coupling with diazonium salts due to the higher nucleophilic character (Fig. 1c, down)65. Thus, unsymmetric arylalkyldiazenes which were also interesting are generated after the combination of alkyl radical and diazonium salts.
Results and discussion
Reaction optimizations
We initially select 4-methoxybenzenediazonium salt 1a as the dual-role reagent and commercially available iodocyclopentane 2a as the radical precursor (Table 1). It was found that common inorganic bases such as Cs2CO3, K2CO3 were quite effective, promoting the generation of the coupled product 3a in high yield after 2 h, while the reaction conducted with weaker base, stronger base, or in the absence of base lead to lower efficiency (Table 1, entry 1–5). It was found that the reaction exhibited high efficiency in dark (Table 1, enrty 6). Using polar MeOH as the solvent, the XAT transformation could afford the coupled product 3a in high yield, while other polar solvents, such as MeCN, DMF led to lower yields (Table 1, entried 8–9). Moreover, no desired product was detected when CH2Cl2 was employed as the solvent (Table 1, entry 7). In particular, the reaction was proved to be sensitive to air since poor efficiency was found when the reaction was conducted under air (Table 1, entry 10).
Substrate scope. With optimized conditions in hand, we next turned our focus to explore the generality of this practical amination via XAT process with respect to diazonium salts (Fig. 2). Coupled partners bearing diverse functional substituents at para- position of the benzene ring underwent this mild transformation smoothly, affording the corresponding products in good to excellent yields (3a–e). It was noted that the CF3, a fluorine-containing group that was prevalent in pharmaceuticals, was compatible with the transformation. Electron-withdrawing groups (COOMe, CN, NO2, and C(O)Me) substituted substrates were also evaluated and the corresponding azo-compounds 3g−j were obtained in good yields. In addition, steric hindrance did not affect the efficiency of this established process, and the products 3k−l were obtained with good yields.
Reaction conditions: 1a-l (1.5 mmol, 3.0 equiv), 2a (0.5 mmol), and Cs2CO3 (0.75 mmol, 1.5 equiv) in MeOH (5.0 mL) at 22 °C for 2 h. Isolated yield.
Encouraged by the general applications of various diazonium salts coupling with model alkyl iodide 2a, the transformation towards the scope of the alkyl iodides was then systematically evaluated (Fig. 3). Over-amination usually occurred in the classic SN2 nucleophilic substitution when the corresponding substrates containing two reacted sites. In contrast, primary iodide 2b bearing a chloride atom under our XAT process was chemo-selectively coupled with 1a, thus providing an alternative opportunity to prepare challenging azo-compound 4a and do further diversifications. Similarly, this practical protocol exhibited excellent functional compatibility and efficiency for a wide variety of alkyl iodides, furnishing a series of azo-compound in moderate to good yields. Unactivated alkyne 4b, ethylene ketal derivate 4c, Boc protected amine 4d, fluobenzene 4e and chlorobenzene derivate 4f could participate well in the two components coupling, and the products were isolated in moderate to good yields. Alkyl iodides containing electron-withdrawing groups (CN, NO2, CHO, C(O)Me, COOMe, and amide) were screened and the desired products 4g−l were generated in good yields. Likewise, a number of functionalized azo compounds were obtained after simple column purification through this mild and efficient strategy. The chemistry was then applied to the substrates bearing long-chain or cyclic aliphatic alkanes and enabled the amination to give the corresponding products 4m, 4r, 4u, 4y−aa, 4ae−af in good to excellent yields. In particular, coupling of the model diazonium salt 1a with heterocyclic iodides were successfully achieved, providing a practical route to access structure-varied azo-compounds 4n−q, 4s−t, 4v−w which might not be easily synthesized by other reported means. It was worth noting that the single crystal structure of compound 4s showed that the diazo group located at the trans-position of the aryl groups (for details, see the Supplementary Information). Moreover, alkyl iodides contained ethylene ketal, adamantane and ester were competent coupling partners, furnishing the desired products 4x, 4ab, and 4ag−ah with high efficiency. Iodinated N-Boc and Ts protected amine 4ai was also comparable as well as iodinated TBS-protected primary alcohol 4ad and free alcohol 4ac, resulting in good conversions. Finally, late-stage amination of complex molecule such as menthol was achieved, illustrating the potential synthetic utility of this practical XAT process.
Reaction conditions: 1a (1.5 mmol, 3.0 equiv), 2b–aj (0.5 mmol, 1.0 equiv), and Cs2CO3 (0.75 mmol, 1.5 equiv) in MeOH (5.0 mL) at 22 °C for 2 h. Isolated yield.
The construction of tertiary C(sp3)-N bonds is still a recognized challenge in traditionally synthetic chemistry, here a wide range of tertiary alkyl iodides which were conveniently prepared from corresponding alcohols in one step could couple well with our model substrate 1a as shown in Fig. 4. A wide variety of functional groups including Cl, Br, and I were tolerated under this mild transformation, resulting in good to excellent yields of the products 6a–f. Heteroaryl iodides 5g–h were also investigated, affording the final products 6g–h in good to excellent yields. Excellent chemo-selectivity was also obtained when the terminal position of the tertiary alkyl iodide was installed with a bromide atom, and product 6i was isolated in yield. Finally, cyclic alkyl iodides 5j–l were also suitable for the XAT process with high efficiency, demonstrating excellent compatibility on the substrates scope. At this point it should be noted that our practical amination from alkyl iodides through XAT process provides a practical route to construct a series of C(sp3)-N bonds under mild and reaction conditions.
Reaction conditions: 1a (1.5 mmol, 3.0 equiv), 6a–l (0.5 mmol, 1.0 equiv), and Cs2CO3 (0.75 mmol, 1.5 equiv) in MeOH (5.0 mL) at 22 °C for 2 h. Isolated yield.
To illustrate the synthetic potential of this practical amination of alkyl iodides, a gram-scale reaction was carried out with the alkyl iodide 5j and model diazonium salts 1a under the standard reaction conditions (Fig. 5a). The coupled product 6j was successfully isolated in 89% yield on 5.0 mmol after simple column chromatography purification. Continuous-flow coupling on 10.0 mmol was further explored by simply switching the base to Et3N due to the poor solubility of diazonium salts 1a and Cs2CO3 in MeOH and the solvent to MeCN, respectively. As a consequence, the corresponding product 3a was obtained in 73% yield (1.5 g) after purification under these mild reaction conditions. Thus, the XAT reaction could be scaled up easily in either flask or continuous-flow system, demonstrating the practicality and potential application of the method.
a 5.0 mmol scale in flask conditions. b 10.0 mmol scale in flow conditions.
Synthetic applications
Two steps involving further purification in the synthesis of the diazonium salts 1a in EtOH and subsequent amination via XAT we established were successfully performed and the corresponding product 3a was generated in comparable yields (Fig. 6a). Late-stage amination of a more complex molecule was also tested and the reaction underwent smoothly with high efficiency, showing the general applicability of this method (Fig. 6b). Furthermore, The N=N bond of the azo product 6j could be successfully transformed into NH2 in the presence of Pd/C and H2 (Fig. 6c). Fischer indole synthesis by the straightforward conversion of our XAT products into the functionalized indoles 9 and 10 in high yield was achieved in the presence of p-toluenesulfonic acid monohydrate (Fig. 6d). Melatonin played a critical role in the mitigation of sleeping disorders and a four-step process to prepare Melatonin has been well developed from the primary alkyl iodide 2m (Fig. 6e). 2.0 mmol scale reaction to generate the corresponding product 4l in 76% isolated yield by employing our well-established transition-metal-free amination method was successfully conducted. Fischer indole formation, and followed traditional hydrazinolysis of the phthaloyl group led to the generation of the free amine, which was further treated with acetyl chloride in the presence of Et3N and the melatonin 12 could be isolated in 74% yield (1.0 mmol scale, two steps).
a Reaction from amine: 1.0 mmol based on alkyl iodide. b Late-stage modification of complex molecule. c Formation of free amine from deprotection by Pd/C. d p-Toluenesulfonic acid monohydrate promoted indole synthesis. e Melatonin synthesis.
Mechanistic study
To seek more insights into the mechanism of this mild and practical amination of alkyl iodides, several mechanistic experiments were performed (Fig. 7). To identify whether radicals are generated in the current XAT process, radical scavenger such as TEMPO was introduced as the additives to the reaction mixture. The coupled product 3a was not observed and this result suggested a radical process was involved in this transformation (Fig. 7a). Next, radical clock experiments were further performed, delivering the corresponding products 14 (ring-closed) and 15 (ring-open) in 56% and 25% yield, respectively (Fig. 7b, c). To validate whether the light has a big impact on the XAT process, the control experiment “in dark” indicated the light did not play a significant role in the transformation since the efficiency was not affected according to the 1H NMR (Fig. 7d). Since the color of the reaction mixture changed to red immediately after the addition of the base such as Cs2CO3 due to the strong interaction between the diazonium salts and base (Fig. 7e). A series of UV/vis absorption spectroscopy studies were conducted to help understanding the mechanism. UV/vis absorption of the individual starting materials including base or combination of iodocyclopentane 2a and Cs2CO3 were recorded, and the corresponding peaks of the absorption spectroscopy remained unchanged (Fig. 7e, right). However, a larger redshift of the mixture of diazonium salts 1a and Cs2CO3 was observed, illustrating a stronger interaction between the diazonium salts 1a and Cs2CO3, or the diazonium salts 1a could be activated by a base such as Cs2CO3 (Fig. 7e, left). Moreover, the redshift disappeared shortly after quick addition of iodocyclopentane 2a into the mixture of the diazonium salts 1a and Cs2CO3, indicating the alkyl iodide might react fast with the “active” radical species generated from the diazonium salts and base. Importantly, 1-iodo-4-methoxybenzene 17 was isolated in quant yield, which supports that the aryl radical could abstract the iodine atom from the corresponding alkyl iodide in the reaction (Fig. 7f). The diazoether 18 which could be formed in the alcoholic media under basic conditions66,67 was successfully subjected to the coupling with alkyl iodide 2a in the absence of base (Fig. 7g). Consequently, the desired product 3i was detected in 32% 1H NMR yield and GC-MS (For details, see the Supplementary Information).
a Radical trapping experiment by employing TEMPO. b Radical clock reaction: ring-closed experiment. c Radical clock reaction: ring-open experiment. d Control experiment. e UV experiments. f Isolation of side product. g Diazoether used for the formation of 3i. h Proposed mechanism.
Based on the results we achieved above and related reports58,59,68, a proposed mechanism was outlined in Fig. 7h: The first step of the reaction could be the generation of diazoether from corresponding diazonium salt in the presence of base such as Cs2CO355,64. Then it underwent homolytic cleavage of “N-O” bond, resulting in the release of nitrogen gas immediately along with the formation of aryl radical since number of bubbles were obviously observed and the color of the reaction mixture was changed to orange (Fig. 7e, UV experiments) after addition of the base55. The active alkyl radical and aryl iodide were formed efficiently via the abstraction of an iodine atom from an alkyl iodide by “in situ” generated aryl radical. Trapping by a diazonium ion, the active alkyl radical could transform into the nitrogen radical cation, which was quenched by the hydroxymethyl radical generated from the HAT process between a methoxyl radical and methanol (for detailed discussion and density functional theory (DFT) calculation, see the Supplementary Information and Supplementary Data 1).
Limitations of the current method
To further expand the scope of this process, The coupling reaction bromocyclopentane 19 and chlorocyclopentane 20 were investigated as the radical precursor. However, >95% recovery of the starting materials 19 and 20 was observed with the full decomposition of the diazonium salts under current reaction conditions (Fig. 8). Since the efficiency in XAT of different alkyl halides can be varied according to the BDE1. As a result, the relative rates for halogen-atom abstractions were determined by the strength of the C-halogen bonds, and the result of our experiments also supports that the trend of halogen-atom abstractions is iodides>bromides>chlorides1,69,70.
The results employing cyclopentyl chloride, bromide, and iodide as alkyl partners in our XAT transformation and BDE difference between them.
In summary, we reported a transition-metal-free strategy for the synthesis of diverse azo-compounds via practical XAT process between diazonium salts and alkyl iodides under mild reaction conditions. Moreover, the diazonium salts were confirmed to act as both oxidants and radical acceptors in redox-neutral reactions. Initial mechanistic experiments and DFT calculation supported this practical amination undergoing generation of aryl radical from diazonium salts promoted by suitable base, XAT (halogen-atom transfer) process from alkyl iodide and aryl radical, and final coupling reaction between alkyl radical with diazonium salts to deliver functionalized azo-compounds. Detailed experiments on the in-situ formation of aryl radicals and other interesting transformations are being explored and these results will be reported in the future.
Methods
General procedure for the amination of alkyl iodides and diazonium tetrafluoroborate
A 25-mL glass vial fitted with a stirring bar was charged with diazonium tetrafluoroborate (1.50 mmol, 3.00 equiv) and Cs2CO3 (244 mg, 0.750 mmol, 1.50 equiv). The mixture was evacuated and backfilled with nitrogen three times. Then the alkyl iodide (0.500 mmol, 1.00 equiv) and MeOH (5.00 mL) were added under nitrogen. The mixture was allowed to stir at 22 °C for 2 h. After the completion of reaction, the reaction mixture was poured into H2O (50.0 mL) and extracted with EtOAc (20.0 mL × 3). The combined organic layers were washed with H2O (20.0 mL), dried over Na2SO4, and filtered. The solvent was removed by rotary evaporation and the residue was purified by flash silica gel chromatography (Caution: alkyl-aryl azo-compounds are usually not stable in the solution of organic solution such as CH2Cl2, CDCl3 and should be handled carefully). Full experimental details and characterization of new compounds in this study are provided in the Supplementary Information.
Data availability
The authors declare that all the data supporting this study, including the experimental details, data analysis, and spectra for all unknown compounds, see Supplementary Files. All data underlying the findings of this work are available from the corresponding author upon request. The X-ray crystallographic coordinates for structures reported in this study have been deposited at the Cambridge Crystallographic Data Centre (CCDC), under deposition number 2181806 (4s). These data are provided free of charge by the joint Cambridge Crystallographic Data Centre and Fachinformationszentrum Karlsruhe Access Structures service www.ccdc.cam.ac.uk/structures.
References
Juliá, F., Constantin, T. & Leonori, D. Applications of halogen-atom transfer (XAT) for the generation of carbon radicals in synthetic photochemistry and photocatalysis. Chem. Rev. 122, 2292–2352 (2022).
Sammes, P.G. Photochemistry of the C-X group. The Carbon—Halogen Bond. 1973, 747–794 (1973).
Kimura, K. & Nagakura, S. n→σ* absorption spectra of saturated organic compounds containing bromine and iodine. Spectrochim. Acta 17, 166–183 (1961).
Kavita, K., Das, P.K. Photodissociation of C6H5I, C6F5I, and related iodides in the ultraviolet. J. Chem. Phys. 117, 2038–2044 (2002)
Bissember, A. C., Lundgren, R. J., Creutz, S. E., Peters, J. C. & Fu, G. C. Transition-metal-catalyzed alkylations of amines with alkyl halides: photoinduced, copper-catalyzed couplings of carbazoles. Angew. Chem. Int. Ed. 52, 5129–5133 (2013).
Kainz, Q. M. et al. Asymmetric copper-catalyzed C-N cross-couplings induced by visible light. Science 351, 681–684 (2016).
Bartoszewicz, A., Matier, C. D. & Fu, G. C. Enantioconvergent alkylations of amines by alkyl electrophiles: copper-catalyzed nucleophilic substitutions of racemic α-halolactams by indoles. J. Am. Chem. Soc. 141, 14864–14869 (2019).
Cho, H., Suematsu, H., Oyala, P. H., Peters, J. C. & Fu, G. C. Photoinduced, copper-catalyzed enantioconvergent alkylations of anilines by racemic tertiary electrophiles: synthesis and mechanism. J. Am. Chem. Soc. 144, 4550–4558 (2022).
Fu, G. C. Transition-metal catalysis of nucleophilic substitution reactions: a radical alternative to SN1 and SN2 processes. Acs. Cent. Sci. 3, 692–700 (2017).
Creutz, S. E., Lotito, K. J., Fu, G. C., Peters, J. C. & Photoinduced Ullmann, C.-N. Coupling: demonstrating the viability of a radical pathway. Science 338, 647–651 (2012).
Liang, Y., Zhang, X. & MacMillan, D. W. C. Decarboxylative sp3 C–N coupling via dual copper and photoredox catalysis. Nature 559, 83–88 (2018).
Mao, R., Frey, A., Balon, J. & Hu, X. Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis. Nat. Catal. 1, 120–126 (2018).
Dow, N. W., Cabré, A. & MacMillan, D. W. C. A general N-alkylation platform via copper metallaphotoredox and silyl radical activation of alkyl halides. Chem 7, 1827–1842 (2021).
Kavita, K. & Das, P. K. Photodissociation of C6H5I, C6F5I, and related iodides in the ultraviolet. J. Chem. Phy. 117, 2038–2044 (2002).
Baguley, P. A. & Walton, J. C. Flight from the tyranny of tin: the quest for practical radical sources free from metal encumbrances. Angew. Chem. Int. Ed. 37, 3072–3082 (1998).
Carey, F.A., Sundberg, R.J. Free Radical Reactions. Advanced Organic Chemistry: Part A: Structure and Mechanisms. Springer US: Boston, MA, 2007, 965–1071.
Constantin, T. et al. Aminoalkyl radicals as halogen-atom transfer agents for activation of alkyl and aryl halides. Science 367, 1021–1026 (2020).
Zhao, H. et al. Merging halogen-atom transfer (XAT) and cobalt catalysis to override e2-selectivity in the elimination of alkyl halides: a mild route toward contra-thermodynamic olefins. J. Am. Chem. Soc. 143, 14806–14813 (2021).
Zhang, Z., Górski, B. & Leonori, D. Merging halogen-atom transfer (XAT) and copper catalysis for the modular Suzuki–Miyaura-type cross-coupling of alkyl iodides and organoborons. J. Am. Chem. Soc. 144, 1986–1992 (2022).
Górski, B., Barthelemy, A.-L., Douglas, J. J., Juliá, F. & Leonori, D. Copper-catalysed amination of alkyl iodides enabled by halogen-atom transfer. Nat. Catal. 4, 623–630 (2021).
Constantin, T., Juliá, F., Sheikh, N. S. & Leonori, D. A case of chain propagation: α-aminoalkyl radicals as initiators for aryl radical chemistry. Chem. Sci. 11, 12822–12828 (2020).
Neff, R. K. et al. Generation of halomethyl radicals by halogen atom abstraction and their addition reactions with alkenes. J. Am. Chem. Soc. 141, 16643–16650 (2019).
Su, Y.-L. et al. α-amino radical-mediated diverse difunctionalization of alkenes: construction of C–C, C–N, and C–S bonds. ACS. Catal. 10, 13682–13687 (2020).
Liu, X.-G., Dong, C.-S., Li, F. & Zhang, B. Manganese-mediated direct functionalization of hantzsch esters with alkyl iodides via an aromatization–dearomatization strategy. Org. Lett. 23, 4002–4007 (2021).
Jamatia, R., Mondal, A. & Srimani, D. Visible-light-induced manganese-catalyzed reactions: present approach and future prospects. Adv. Synth. Catal. 363, 2969–2995 (2021).
Cai, A., Yan, W., Wang, C. & Liu, W. Copper-catalyzed difluoromethylation of alkyl iodides enabled by aryl radical activation of carbon–iodine bonds. Angew. Chem. Int. Ed. 60, 27070–27077 (2021).
Mailyan, A. K. et al. Cutting-edge and time-honored strategies for stereoselective construction of C–N bonds in total synthesis. Chem. Rev. 116, 4441–4557 (2016).
Vitaku, E., Smith, D. T. & Njardarson, J. T. Analysis of the structural diversity, substitution patterns, and frequency of nitrogen heterocycles among U.S. FDA approved pharmaceuticals. J. Med. Chem. 57, 10257–10274 (2014).
Trowbridge, A., Walton, S. M. & Gaunt, M. J. New strategies for the transition-metal catalyzed synthesis of aliphatic amines. Chem. Rev. 120, 2613–2692 (2020).
Zhao, Y. & Xia, W. Recent advances in radical-based C–N bond formation via photo-/electrochemistry. Chem. Soc. Rev. 47, 2591–2608 (2018).
Shao, X., Li, K. & Malcolmson, S. J. Enantioselective synthesis of anti-1,2-diamines by Cu-catalyzed reductive couplings of azadienes with aldimines and ketimines. J. Am. Chem. Soc. 140, 7083–7087 (2018).
Zhou, P., Shao, X. & Malcolmson, S. J. A diastereodivergent and enantioselective approach to syn- and anti-diamines: development of 2-azatrienes for Cu-catalyzed reductive couplings with imines that furnish allylic amines. J. Am. Chem. Soc. 143, 13999–14008 (2021).
Jung, W.-O. et al. Enantioselective iridium-catalyzed allylation of nitroalkanes: entry to β-stereogenic α-quaternary primary amines. J. Am. Chem. Soc. 143, 9343–9349 (2021).
Xiong, T. & Zhang, Q. New amination strategies based on nitrogen-centered radical chemistry. Chem. Soc. Rev. 45, 3069–3087 (2016).
Niu, D. & Buchwald, S. L. Design of modified amine transfer reagents allows the synthesis of α-chiral secondary amines via CuH-catalyzed hydroamination. J. Am. Chem. Soc. 137, 9716–9721 (2015).
Zhu, S., Niljianskul, N. & Buchwald, S. L. Enantio- and regioselective CuH-catalyzed hydroamination of alkenes. J. Am. Chem. Soc. 135, 15746–15749 (2013).
Waser, J. & Carreira, E. M. Convenient synthesis of alkylhydrazides by the cobalt-catalyzed hydrohydrazination reaction of olefins and azodicarboxylates. J. Am. Chem. Soc. 126, 5676–5677 (2004).
Lang, K., Torker, S., Wojtas, L. & Zhang, X. P. Asymmetric induction and enantiodivergence in catalytic radical C–H amination via enantiodifferentiative H-atom abstraction and stereoretentive radical substitution. J. Am. Chem. Soc. 141, 12388–12396 (2019).
Shi, F., Cui, X. Chapter 1 - N-alkyl amine synthesis by catalytic alcohol amination. In: Shi F, Cui X (eds). Catalytic Amination for N-Alkyl Amine Synthesis. Academic Press, 2018, 1–58.
Jerca, F. A., Jerca, V. V. & Hoogenboom, R. Advances and opportunities in the exciting world of azobenzenes. Nat. Rev. Chem. 6, 51–69 (2022).
Crespi, S., Simeth, N. A. & König, B. Heteroaryl azo dyes as molecular photoswitches. Nat. Rev. Chem. 3, 133–146 (2019).
Polanc, S. New synthetic applications and biological activity of diazenes. J. Heterocycl. Chem. 42, 401–412 (2005).
Skubi, K. L., Blum, T. R. & Yoon, T. P. Dual catalysis strategies in photochemical synthesis. Chem. Rev. 116, 10035–10074 (2016).
Trofimov, A., Chernyak, N. & Gevorgyan, V. Dual role of alkynyl halides in one-step synthesis of alkynyl epoxides. J. Am. Chem. Soc. 130, 13538–13539 (2008).
Park, Y., Schindler, C. S. & Jacobsen, E. N. Enantioselective aza-sakurai cyclizations: dual role of thiourea as h-bond donor and lewis base. J. Am. Chem. Soc. 138, 14848–14851 (2016).
Schröder, N., Lied, F. & Glorius, F. Dual role of Rh(III) catalyst enables regioselective halogenation of (electron-rich) heterocycles. J. Am. Chem. Soc. 137, 1448–1451 (2015).
Mo, F., Qiu, D., Zhang, L. & Wang, J. Recent development of aryl diazonium chemistry for the derivatization of aromatic compounds. Chem. Rev. 121, 5741–5829 (2021).
Mo, F., Dong, G., Zhang, Y. & Wang, J. Recent applications of arene diazonium salts in organic synthesis. Org. Biomol. Chem. 11, 1582–1593 (2013).
Mahouche-Chergui, S., Gam-Derouich, S., Mangeney, C. & Chehimi, M. M. Aryl diazonium salts: a new class of coupling agents for bonding polymers, biomacromolecules and nanoparticles to surfaces. Chem. Soc. Rev. 40, 4143–4166 (2011).
Bernard, M.-C. et al. Organic layers bonded to industrial, coinage, and noble metals through electrochemical reduction of aryldiazonium salts. Chem. Mater. 15, 3450–3462 (2003).
Hodgson, H. H. The sandmeyer reaction. Chem. Rev. 40, 251–277 (1947).
Wang, X. et al. Silver-mediated trifluoromethylation of aryldiazonium salts: conversion of amino group into trifluoromethyl group. J. Am. Chem. Soc. 135, 10330–10333 (2013).
Zhang, F.-G., Chen, Z., Cheung, C. W. & Ma, J.-A. Aryl diazonium salt-triggered cyclization and cycloaddition reactions: past, present, and future. Chin. J. Chem. 38, 1132–1152 (2020).
Liu, H.-N., Cao, H.-Q., Cheung, C. W. & Ma, J.-A. Cu-mediated expeditious annulation of alkyl 3-aminoacrylates with aryldiazonium salts: access to alkyl N2-aryl 1,2,3-triazole-carboxylates for druglike molecular synthesis. Org. Lett. 22, 1396–1401 (2020).
Peng, X., Xiao, M.-Y., Zeng, J.-L., Zhang, F.-G. & Ma, J.-A. Construction of difluoromethylated tetrazoles via silver-catalyzed regioselective [3 + 2] cycloadditions of aryl diazonium salts. Org. Lett. 21, 4808–4811 (2019).
Mo, F., Qiu, D., Zhang, Y. & Wang, J. Renaissance of sandmeyer-type reactions: conversion of aromatic C–N bonds into C–X bonds (X = B, Sn, P, or CF3). Acc. Chem. Res. 51, 496–506 (2018).
Hari, D. P. & König, B. The photocatalyzed meerwein arylation: classic reaction of aryl diazonium salts in a new light. Angew. Chem. Int. Ed. 52, 4734–4743 (2013).
Kindt, S., Wicht, K. & Heinrich, M. R. Base-induced radical carboamination of nonactivated alkenes with aryldiazonium salts. Org. Lett. 17, 6122–6125 (2015).
Kindt, S., Wicht, K. & Heinrich, M. R. Thermally induced carbohydroxylation of styrenes with aryldiazonium salts. Angew. Chem. Int. Ed. 55, 8744–8747 (2016).
An, Y. & Wu, J. Synthesis of tetrahydropyridine derivatives through a reaction of 1,6-enynes, sulfur dioxide, and aryldiazonium tetrafluoroborates. Org. Lett. 19, 6028–6031 (2017).
Kurandina, D. et al. Transition-metal- and light-free directed amination of remote unactivated C(sp3)–H bonds of alcohols. J. Am. Chem. Soc. 141, 8104–8109 (2019).
Angnes, R. A., Potnis, C., Liang, S., Correia, C. R. D. & Hammond, G. B. Photoredox-catalyzed synthesis of alkylaryldiazenes: formal deformylative C–N bond formation with alkyl radicals. J. Org. Chem. 85, 4153–4164 (2020).
Ghosh, I., Marzo, L., Das, A., Shaikh, R. & König, B. Visible light mediated photoredox catalytic arylation reactions. Acc. Chem. Res. 49, 1566–1577 (2016).
Abrams, R., Lefebvre, Q. & Clayden, J. Transition metal free cycloamination of prenyl carbamates and ureas promoted by aryldiazonium salts. Angew. Chem. Int. Ed. 57, 13587–13591 (2018).
Citterio, A. & Minisci, F. Free-radical diazocoupling. A new general reaction of diazonium salts. J. Org. Chem. 47, 1759–1761 (1982).
DeTar, D. F. & Kosuge, T. Mechanisms of diazonium salt reactions. VI. The reactions of diazonium salts with alcohols under acidic conditions; evidence for hydride transfer. J. Am. Chem. Soc. 80, 6072–6077 (1958).
DeTar, D. F. & Turetzky, M. N. The mechanisms of diazonium salt reactions. I. The products of the reactions of benzenediazonium salts with methanol. J. Am. Chem. Soc. 77, 1745–1750 (1955).
Witzel, S. et al. Excitation of aryl cations as the key to catalyst-free radical arylations. Cell. Rep. Phys. Sci. 2, 100325 (2021).
Newcomb, M., Sanchez, R. M. & Kaplan, J. Fast halogen abstractions from alkyl halides by alkyl radicals. Quantitation of the processes occurring in and a caveat for studies employing alkyl halide mechanistic probes. J. Am. Chem. Soc. 109, 1195–1199 (1987).
Curran, D. P., Bosch, E., Kaplan, J. & Newcomb, M. Rate constants for halogen atom transfer from representative.alpha.-halo carbonyl compounds to primary alkyl radicals. J. Org. Chem. 54, 1826–1831 (1989).
Acknowledgements
We are grateful for the National Science Foundation of China (22001051), Hangzhou Leading Innovation and Entrepreneurship Team Project (TD2020015), and start-up funding of Hangzhou Normal University for financial support. We thank Dr. Chunqi Sheng (Hangzhou Normal University) for the assistance with IR analysis, Dr. Hong Dong (Hangzhou Normal University) for HRMS analysis, and Prof Xuqiong Xiao for X-ray analysis. We also greatly thank Prof Yangyang Shen (Xi’an Jiaotong University) for the helpful discussion.
Author information
Authors and Affiliations
Contributions
X.X.S., H.L., C.S.W., L.W.X., and K.G. conceived and supervised the projects. J.Z., C.S.W., Y.Z., G.Q.C, and X.X.S. performed the experiments and analyzed the data. S.F.N.; Q.X.L., C.M. performed the DFT calculation. X.X.S., H.L., M.J., C.S.W., S.F.N.; L.W.X., and K.G. prepared the manuscript with feedback from all authors.
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Nature Communications thanks Jianbo Wang, and the other, anonymous, reviewers for their contribution to the peer review of this work.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Zhang, J., Jiang, M., Wang, CS. et al. Transition-metal free C–N bond formation from alkyl iodides and diazonium salts via halogen-atom transfer. Nat Commun 13, 7961 (2022). https://doi.org/10.1038/s41467-022-35613-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467-022-35613-7
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.
