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 (1)H NMR, (13)C 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.

“Simple” enols are defined as compounds with substituents, such as hydrogen, alkyl, or aryl groups, bounded to their double-bond. They are known as very unstable compounds. Enols are usually short-lived as a result of their kinetically and thermodynamically unstable properties compared to their keto forms, so they are usually present as transient intermediates at very low concentrations in various organic reactions involving aldehydes and ketones123. Enol compounds have been under active investigations for over one century456, not only from the viewpoints of synthesis789 and their spectroscopic behavior10 but also because of their roles in DNA damage11121314 and biological function151617. However, most of the recent investigations are focused on the spectroscopy equilibrium between keto and enol formation and the factors influencing their equilibrium1819202122. There are still only a few reports on the synthesis of stable enol in the literature.

Early efforts to synthesize stable enols failed because of the limited synthetic means and the misunderstanding between the stability and structure of enols. Remarkable progress in the synthesis of simple enols in early years was achieved by Capon′s2324 and Kresge′s groups2526. Later, scientists also made some contributions in this area272829. However, in literature, with an equilibrium with its keto tautomers, enols are always obtained as mixtures with their carbonyl isomers. Furthermore, the existence of these enols are conditional, usually in specific solvent303132, at low temperature33, in gas form3435, or in surrounding capsule cage36. The concentrations of the enols are usually too low that they have to be determined indirectly. Moreover, most of these enols are stabilized by aryl272829 or existed as cyclic structures373839, they rapidly tautomerized to their carbonyl isomers as a result of their kinetic instability under inappropriate conditions232440. Synthesis of stable acyclic aliphatic enols is still a challenge for chemists.

In 1922, Diels′ group reported the possibility of the existence of enol, but they were not able to confirm it41. They neither characterized the structure of the products of acetylacetone with DEAD nor discussed the relationship between the stability and structure of enols. After Diels′ report, in 1980, Nelson reported a Nickel-catalyzed Michael addition of β-carbonyl ester with azodicarboxylate, to give 1,3-dicarbonyl compounds42. Later, other catalysts, such as InCl3 and SiO2, were used in similar reactions to afford 1,3-dicarbonyl compounds434445. However, no stable enol compounds were reported in these reactions. Until 2010, Lawrence described the first example of a stable phenylogous enol, resulting from an extended keto-enol tautomerization across a benzene ring. The enol has been isolated, and its structure was proved by X-ray crystallography39.

In this manuscript, an efficient way to synthesize very stable hydrazine substituted enol is provided and series of stable aliphatic solid enols, which are different from Lawrence′s phenylogous enol, were obtained and studied. These enols are remarkably stable under open atmosphere, and no tautomerization to their carbonyl isomers were observed. The relationship between structure and the stability of the enol was investigated. Gaussian 09 calculations had been carried out, proving that enol forms are more superior than their keto forms in energy. These enol structures are unambiguously confirmed by 1H NMR, 13C NMR, MS, IR spectra partly by single crystal X-ray 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 1H NMR spectra. Then, we did rotons exchange experiments, signal at 12.11 ppm disappeared when this product was dissolved in CDCl3 with a drop of D2O, indicating the hydroxyl group is existent in the product. Besides, absorbtions at about 3280 cm−1 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 Cs2CO3 were employed at the same time in this reaction (entries 15), compared with using KOtBu, K2CO3 (entries 12, 13) or only use of Cs2CO3(entries 14).

Figure 1

Optimized conditions for the reaction of ethyl acetoacetate 1a with DEAD 2aa.

With the optimized conditions in hand, we then investigated the scope of substitutents on this reaction. Various β-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 R1 or R2, because these carbonyl esters readily participated to react with DEAD. However, yields are a little bit lower when substitutents are bulky groups such as 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 R1, R2, R3 have limited impact on the yields.

Figure 2

Expansion of β-carbonyl esters 1 with azodicarboxylates 2a.

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 β-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).

Figure 3

Possible intramolecular hydrogen bonds in A.

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 O1H group and O2, with a distance of 1.789 Å are close enough to form intramolecular hydrogen bonds. However, the distance of N2H group with O3 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 1H NMR. The examination of 3a in CDCl3, CD3OD, C6D6, CD3COCD3, CD3CN and CD3SOCD3 showed that enol form products can be well maintained in aprotic solvent, such as CDCl3, C6D6 and CD3CN. 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 CD3COCD3 and CD3SOCD3. 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 CD3COCD3 or CD3SOCD3 was moved and CDCl3 was added, its 1H NMR data is as same as the data of 3a which was directly collected in CDCl3. Although protophilic solvent, such as CD3COCD3 and CD3SOCD3, can partly disrupt the intramolecular hydrogen bonds in these enols, enol forms remain predominant from their 1H 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 CD3OD (proton exchanged).

Figure 4

The X-ray crystal structure of compound 3a.

Intramolecular hydrogen bond is displayed in dashed lines.

Computationally study about enol is one topic attracted many chemists4647484950. 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 carbon-carbon double bond in 3a, p-π conjugation and π-π conjugation are possible, which strongly dispersed the electrons. When 3a tautomerized to 3a′, however, p-π conjugation and π-π 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 3a′ as the model structure to perform the Gaussian 09 calculations (Fig. 5). The optimized structure is quite in accord with the single crystal X-ray structure (Fig. 6). The results showed that energies of 3a are lower than 3a′(H − H = −9.6 Kcal/mol, G −G = −8.8 Kcal/mol in gas form, H −H = −6.9 Kcal/mol, G −G = −6.2 Kcal/mol in the solvent model of CH2Cl2 ) (See supporting information), supporting that the superiority of the enol form of 3a is obvious when it is compared with its keto form isomer 3a′.

Figure 5

The model structures of β-carbonyl ester 3a and its keto form 3a′.

Figure 6

The optimized structure of 3a.

To confirm that the intramolecular hydrogen bond is strong enough to maintain the enol form, we expanded the substrate from β-carbonyl esters to β-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, 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 1H NMR spectra of 5c with groups Bu is stronger than the second signal in 1H NMR spectra of 5b with groups 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 13C 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.

Figure 7

Expansion of β-carbonyls 4 with azodicarboxylates 2a.

Thus, product 5a was easily obtained as the only product in enol form. Because only one signal was determined through the chiral column on HPLC and signal at 16.02 ppm disappeared while deuterated with D2O in CDCl3, it indicates that the product 5a is also an enol form with overwhelming superiority.

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 5a′ 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 5a′ (H − H = −9.4 Kcal/mol, G − G = −9.5 Kcal/mol in gas form, H − H = −6.5 Kcal/mol, G −G = −6.7 Kcal/mol in the solvent model of CH2Cl2), 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.

Figure 8

The X-ray crystal structure of compound 5a.

Intramolecular hydrogen bond is displayed in dashed lines.

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-π conjugation and π-π 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 –NO2,–CN, Me and CF3 to react with DEAD (Fig. 9). Substrates with electron withdrawing group, such as, CN and NO2 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 Cs2CO3, 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 condition51. For the same reason entry 4 can't work either.

Figure 9

Expansion of carbonyls 6 with DEADa.

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-π conjugation and π-π 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 1H NMR, 13C 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 (CH2Cl2), the solvent medium in the experiments. The single point energies were also computed using the M05-2X method with the 6–311++G** 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 (1H NMR) and 100 MHz (13C NMR). TMS was used as an internal standard and CDCl3 was used as the solvent 1H NMR data were reported as follows: chemical shifts in ppm downfield from tetramethylsilane, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet and br = broad), J = 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 CH2Cl2, azodicarboxylates (1.0 mmol ) was added. And followed by the addition of quinine (0.02 mmol) and Cs2CO3 (0.02 mmol). The mixture was stirred for 4–8 h at room temperature. The reaction was monitored by TLC (ethyl acetate : petroleum ether = 1:5 V/V). After evaporation of the solvents, the residue was purified by silica gel column chromatography (ethyl acetate : petroleum ether = 1:5 V/V). Full experimental details and the characterization data for all the compounds are given in the Supplementary Information.

Author Contributions

Yu-Qiang Zhou and Nai-Xing Wang wrote the main manuscript text and Yanfeng Dang and Zhi-Xiang Wang prepared figure 6. All authors reviewed the manuscript.