Stable acyclic aliphatic solid enols: synthesis, characterization, X-ray structure analysis and calculations

A synthetic approach to stable enols was introduced and series of acyclic aliphatic solid enols were obtained and characterized. Relationship between the structure and the stability of these enols was discussed. Gaussian 09 calculations had been carried out to rationalize the stability of the enols. These enol structures were confirmed by 1H NMR, 13C NMR, MS, IR, partly by single crystal X-ray structure analysis and the protons exchange experiments. This work showed that very stable acyclic aliphatic enols can be synthesized efficiently without any purification.

structure analysis and other methods. This work showed some enol compounds can be synthesized easily without any purification. We believe this complete study on the stable enols will bring a new insight on the stability of this important species in organic synthesis.

Results
We used ethyl acetoacetate as a standard substrate to react with DEAD in the presence of quinine and expected to get product bearing one chiral centre. After the pure product was obtained, we detected it through a chiral column on HPLC. With only one signal was detected by the chiral column, we thought a product with very high ee value might be obtained. When we changed the chiral base quinine into an achiral base triethylamine, we thought two signals should be observed via HPLC in the same condition. To our surprise, still only one signal was observed at the same HPLC retention time. And two broad signals at 12.11 ppm and 6.80 ppm were observed in the 1 H NMR spectra. Then, we did rotons exchange experiments, signal at 12.11 ppm disappeared when this product was dissolved in CDCl 3 with a drop of D 2 O, indicating the hydroxyl group is existent in the product. Besides, absorbtions at about 3280 cm 21 were found in IR spetrum. Based on these results, we proposed the product should be enol. This conclusion was subsequently confirmed through many ways.
As initial optimization of the reaction conditions, ethyl acetoacetate 1a and DEAD 2a were chosen as the model substrates. The results are summarized in Fig. 1. Different organic bases, such as diethylamine, triethylamine, DBU, pyrrolidine, L-proline and quinine were tested in dichloromethane (DCM) at room temperature (entries 1-6). It was confirmed that all of the organic bases mentioned can be used as catalysts in this reaction. However, quinine seems to be the best one, because it can offer both the fastest rate and excellent yields with lower catalyst loading. The solvents were subsequently examined, we found DCM is a suitable one among various solvents listed in Fig. 1 (entries 7-11). To our delight, the best result (99%) was achieved when quinine and Cs 2 CO 3 were employed at the same time in this reaction (entries 15), compared with using KOtBu, K 2 CO 3 (entries 12, 13) or only use of Cs 2 CO 3 (entries 14).
With the optimized conditions in hand, we then investigated the scope of substitutents on this reaction. Various b-carbonyl esters and azodicarboxylates were examined, as summarized in Fig. 2. We found that these reactions can be carried out without limitation in the groups R 1 or R 2 , because these carbonyl esters readily participated to react with DEAD. However, yields are a little bit lower when substitutents are bulky groups such as t Bu (94%) (entry 3). Even 3f with Bn group in its structure, 95% yield was achieved (entry 6). All of the reactions performed smoothly when carbonyl esters reacted with several azodicarboxylates (entries 1, 7-9). Although 3g, 3h, 3i were synthesized from substrates with bulky groups, corresponding products were obtained in excellent yields (94-97%)(entries 7-9). In all of cases, the products were obtained with excellent yields, we believe that the groups R 1 , R 2 , R 3 have limited impact on the yields.
With our efforts to understand this reaction, we became interested to know why these enol form products are stable. We decided to study products A obtained from b-carbonyl esters. We found intramolecular hydrogen bonding is very important to the stability of enols. Initially, we thought A could be stabilized by one O-H-O intramolecular hydrogen bond and one N-H-O intramolecular hydrogen bond (Fig. 3).
We speculated that both of these two intramolecular hydrogen bonds were working together to maintain the stability of these enols and disenable the isomerization to their keto isomers. We tried to prove our hypothesis by the single crystal X-ray structure analysis    Fig. 4). From the data of single crystal X-ray structure analysis of compound 3a (CCDC 816568 contains the supplementary crystallographic data for this compound. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif), we could see O 1 H group and O 2 , with a distance of 1.789 Å are close enough to form intramolecular hydrogen bonds. However, the distance of N 2 H group with O 3 is beyond of the range of intramolecular hydrogen bonds. Therefore, O-H-O intramolecular hydrogen bond plays very important role to the enol and it is strong enough to maintain the enol form. This speculation was subsequently proved by performing deuterated solvent study by 1 H NMR. The examination of 3a in CDCl 3 , CD 3 OD, C 6 D 6 , CD 3 COCD 3 , CD 3 CN and CD 3 SOCD 3 showed that enol form products can be well maintained in aprotic solvent, such as CDCl 3 , C 6 D 6 and CD 3 CN. However, some protic solvents and protophilic solvents affected the intramolecular hydrogen bonds in 3a, because second small signals in the enol proton region at 12.0 ppm were found, such as in solvents CD 3 COCD 3 and CD 3 SOCD 3. These additional signals should belong to enol protons which are partly released from previous intramolecular hydrogen bond as a result of the disruption of carbonyl or sulfinyl. It is worth mentioning that when CD 3 COCD 3 or CD 3 SOCD 3 was moved and CDCl 3 was added, its 1 H NMR data is as same as the data of 3a which was directly collected in CDCl 3 . Although protophilic solvent, such as CD 3 COCD 3 and CD 3 SOCD 3 , can partly disrupt the intramolecular hydrogen bonds in these enols, enol forms remain predominant from their 1 H NMR data. Moreover, we are pretty confident that the products are enols since enol signal at 12.11 ppm disappeared when this product was dissolved in CD 3 OD (proton exchanged).
Computationally study about enol is one topic attracted many chemists [46][47][48][49][50] . Energy calculated by the computer is another important factor taken into consideration by our group. Take product 3a for example, as a result of the effect of the intramolecular hydrogen bond, the carbon-carbon double bond is formed (Fig. 5, 3a). With oxygen atom, nitrogen atom and carbonyl bonded to the carboncarbon double bond in 3a, p-p conjugation and p-p conjugation are possible, which strongly dispersed the electrons. When 3a tautomerized to 3a9, however, p-p conjugation and p-p conjugation are not possible because of the barrier of the tertiary carbon. As a result of this, we supposed 3a should have lower energy in theory, which benefits the enol form and stabilizes the enol forms. This hypothesis was proved by the Gaussian 09 calculations in this paper (See supporting information). We chose 3a and its keto form isomer 3a9 as the model structure to perform the Gaussian 09 calculations (Fig. 5). The optimized structure is quite in accord with the single crystal Xray structure (Fig. 6). The results showed that energies of 3a are lower than 3a9(H 3a 2 H 3a9 5 29.6 Kcal/mol, G 3a 2G 3a9 5 28.8 Kcal/mol in gas form, H 3a 2H 3a9 5 26.9 Kcal/mol, G 3a 2G 3a9 5 26.2 Kcal/ mol in the solvent model of CH 2 Cl 2 ) (See supporting information), supporting that the superiority of the enol form of 3a is obvious when it is compared with its keto form isomer 3a9.
To confirm that the intramolecular hydrogen bond is strong enough to maintain the enol form, we expanded the substrate from b-carbonyl esters to b-carbonyl ketone compounds, some enol form products were obtained (Fig. 7). It was pleasant that all the reactions performed very well by carrying out the foregoing condition and all substrates provided high yield products (entries 1-5). Such as, products 5a and 5b were obtained with 99% and 97% yields (entries 1, 2). However, substrates with bulky groups, such as, t Bu, Ph slightly lowered the yields (entries 3-5). It should be mentioned that the size of the central substituent has slightl effect on the formation of the intramolecular hydrogen bonds because additional signals in the enol proton region at 16.0 ppm were found in the spectra of 5b and 5c and the second signal in 1 H NMR spectra of 5c with groups t Bu is stronger than the second signal in 1 H NMR spectra of 5b with groups i Pr. Steric hindrance should lead to a distortion and disrupted intramolecular hydrogen bonds so that the enol proton can partly release from intramolecular hydrogen bond to give an additional signal. For the same reason, additional signals could be found in the 13 C NMR spectrum of 5b and 5c. However, all the products were detected through the chiral column on HPLC, each of them gave one signal, which means the enol form was obtained with overwhelming superiority by the mobile phase of n-Hexane and 2-propanol.
Thus, product 5a was easily obtained as the only product in enol form. Because only one signal was determined through the chiral    Similarly, 5a also have lower energy which benefits the enol form and stabilizes its enol structure. Luckily, this was also proved by the Gaussian 09 calculations when we chose 5a and its keto form isomer 5a9 as the model structure to perform the calculations. The optimized structure is quite similar with the single crystal X-ray structure (See supporting information). The results showed that the energy of 5a is lower than 5a9 (H 5a 2 H 5a9 5 29.4 Kcal/mol, G 3a 2 G 3a9 5 29.5 Kcal/mol in gas form, H 5a 2 H 5a9 5 26.5 Kcal/mol, G 5a 2G 5a9 5 26.7 Kcal/mol in the solvent model of CH 2 Cl 2 ), indicating enol forms are more superior than their keto forms in energy. Enol form structure of product 5a was unambiguously confirmed by the single crystal X-ray structure analysis at last (Fig. 8). (CCDC 849478 contains the supplementary crystallographic data for this compound. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_ request/cif). From the data of single crystal X-ray of 5a, we can find proton H1 is between O1 and O2, the distance of H1 with O1 and the distance of H1 with O2 are close enough to form intramolecular hydrogen bonds. However, the acetoacetate fragment is not completely symmetrical because the distance of H1-O1 and the distance of H1-O2 are not equivalent. And the distance of O1-C2 and O2-C4 are not equivalent either. With a 72.4 deg. angle between C4-C3 and N1-N2, it seems that the hydrazine moiety is not orthogonal with the acetoacetate fragment. But hydrazine with bulky groups should have impact on the structure because it can lead to a deformation. Indeed, large hydrazine substituents could also likely favor the formation of the enol relative to the keto isomer.
In conclusion, three main reasons should be responsible for the stability of enol form. 1) the intramolecular hydrogen bond of O-H-O, 2) the p-p conjugation and p-p conjugation in these compounds.
3) appropriate group is another factor to the enol.
With our efforts to understand the relation between the structure and the stability of enols, we expanded substrates with groups at the beta position to more common groups, such -NO 2 ,-CN, Me and CF 3 to react with DEAD ( Fig. 9). Substrates with electron withdrawing group, such as, CN and NO 2 readily performed with DEAD in the present of quinine, giving 7a and 7b with good yields (entries 1 and 2). Each one of 7a and 7b showed one signal through the chiral column on HPLC, which means two enol form compounds were yielded. However, when we used propiophenone as a substrate to react with DEAD in the presence of quinine and Cs 2 CO 3 , only trace amount of product was determined after 24 h (entry 3). This is probably because the reaction can't be carried out with this condition 51 . For the same reason entry 4 can't work either.

Discussion
As a conclusion, an efficient method to prepare stable enols was introduced and series of acyclic aliphatic solid enols were synthesized. The relationship between structure and the stability of enols was discussed. We found that groups beta to the carbonyl in substrates are important to formation of enols, because these groups could either balance the electron by the p-p conjugation and p-p conjugation or could form intramolecular hydrogen bond with OH. With our method, stable acyclic aliphatic solid enols were easily obtained as only products. Notably, all of the enols synthesized can be stably maintained in normal condition. Gaussian 09 calculations had been carried out by using enols mentioned in this paper and their keto isomers as models structures, proving that enol forms are more predominant than their keto forms in energy. These enol structures are confirmed by 1 H NMR, 13 C NMR, MS, partly by single crystal    X-ray structure analysis and the protons exchange experiments. We believe this is a complete study on an important species in organic synthesis. Further studies about other types of stable enols are currently under investigation and will be presented in a due time.

Methods
All calculations were carried out with the Gaussian 09 programs. The geometrical optimizations of all the complexes were performed using M05-2X with the 6-31G** basis set for all atoms. Frequency calculations at the same level were performed to confirm each stationary point to be a minimum. The free energies of solvation in this study were calculated based on the gas phase optimized structures with the polarizable continuum model (PCM) using UA0 radii. The dielectric constant in the PCM calculations was set to 8.93 to simulate dichloromethane (CH 2 Cl 2 ), the solvent medium in the experiments. The single point energies were also computed using the M05-2X method with the 6-31111G** basis set for all atoms. The report free energies and enthalpies include zero-point energies and thermal corrections calculated at 298.15K and 1 atm.
Unless otherwise noted, materials were used as commercial suppliers. All solvents were purified by standard method. Flash column chromatography was performed using 200-300 mesh silica gel.
Reaction progress was followed by TLC analysis at 254 nm. NMR spectroscopy was performed on 400 MHz spectrometer operating at 400 MHz ( 1 H NMR) and 100 MHz ( 13 C NMR). TMS was used as an internal standard and CDCl 3 was used as the solvent 1 H NMR data were reported as follows: chemical shifts in ppm downfield from tetramethylsilane, multiplicity (s 5 singlet, d 5 doublet, t 5 triplet, q 5 quartet, m 5 multiplet and br 5 broad), J 5 coupling constant. IR spectra were recorded by using KBr optics. All the reagents are used directly from commercial and without further purification.
General procedure for the synthesis of all enols. To a solution of carbonyl compounds (1.0 mmol) in CH 2 Cl 2 , azodicarboxylates (1.0 mmol ) was added. And followed by the addition of quinine (0.02 mmol) and Cs 2 CO 3 (0.02 mmol). The mixture was stirred for 4-8 h at room temperature. The reaction was monitored by TLC (ethyl acetate : petroleum ether 5 1:5 V/V). After evaporation of the solvents, the residue was purified by silica gel column chromatography (ethyl acetate : petroleum ether 5 1:5 V/V). Full experimental details and the characterization data for all the compounds are given in the Supplementary Information.