Optimization of technological conditions for one-pot synthesis of (S)-α-cyano-3-phenoxybenzyl acetate in organic media

Optimization of technological conditions for one-pot synthesis of (S)-α-cyano-3-phenoxybenzyl acetate in organic media 1 2 first-author †E-mail:zhangtz@hzcnc.com; lryang@zju.edu.cn †E-mail:zhangtz@hzcnc.com; lryang@zju.edu.cn zhangtz@hzcnc.com 1 †E-mail:zhangtz@hzcnc.com; lryang@zju.edu.cn †E-mail:zhangtz@hzcnc.com; lryang@zju.edu.cn zhangtz@hzcnc.com 1 School of Material & Chemical Engineering, Zhejiang University, Hangzhou 310027, China School of Material & Chemical Engineering, Zhejiang University, Hangzhou 310027, China School of Food Science, Biotechnology & Environmental Engineering, Zhejiang Gongshang University, Hangzhou 310035, China School of Food Science, Biotechnology & Environmental Engineering, Zhejiang Gongshang University, Hangzhou 310035, China Optically active form of α-cyano-3-phenoxybenzyl (CPB) alcohol, building block of pyrethroid insecticides, was synthesized as its acetate by the combination of anion-exchange resin (D301)-catalyzed transcyanation between m-phenoxybenzaldehyde (m-PBA) and acetone cyanohydrin (AC), and lipase (from Alcaligenes sp.)-catalyzed enantioselective transesterification of the resulting cyanohydrin with vinyl acetate. Through optimizing technological conditions, the catalyzing efficiency was improved considerably compared to methods previously reported. Concentrations of CPB acetate were determined by gas chromatograph. The enantio excess (e.e.) values of CPB acetate were measured by NMR (nuclear magnetic resonance) method. Effects of solvents and temperatures on this reaction were studied. Cyclohexane was shown to be the best solvent among the three tested solvents. 55 °C was the optimal temperature for higher degree of conversion. External diffusion limitation was excluded by raising the rotational speed to 220 r/min. However, internal diffusion could not be ignored, since the catalyst (lipase) was an immobilized enzyme and its particle dimension was not made small enough. The reaction rate was substantially accelerated when the reactant (m-PBA) concentration was as high as 249 mmol/L, but decreased when the initial concentration of m-PBA reached to 277 mmol/L. It was also found that the catalyzing capability of recovered lipase was high enough to use several batches. Study of the mole ratio of AC to m-PBA showed that 2:1 was the best choice. The strategy of adding base catalyst D301 was found to be an important factor in improving the degree of conversion of the reaction from 20% to 80%. The highest degree of conversion of the reaction has reached up to 80%. Biosynthesis α-cyano-3-phenoxybenzyl (CPB) acetate Lipase Optimization Organic media INTRODUCTION 1 Cyanohydrin compounds are useful synthetic intermediates in organic synthesis and are important starting materials for the synthesis of pharmaceuticals (Klibanov, 1990 1990 ). Optically active cyanohydrin esters can be obtained by enzymatic transesterification of racemic cyanohydrins in organic solvent (Wang et al., 1989 1989 ). (S)-α-cyano-3-phenoxybenzyl (CPB) alcohol is an important building block of pyrethroid insecticides and has received increasing interest for use in biological agrochemicals. So, results of study on the technological conditions for the synthesis of (S)-CPB will have practically significance. Inagaki et al.( 1991 1991 ) first proposed a one-pot method to synthesize CPB acetate in an approach to the synthesis of (S)-CPB acetate through in situ racemization of corresponding cyanohydrin formed from m-phenoxybenzaldehyde (m-PBA) and acetone cyanohydrin (AC) by the combination of chemical and biochemical catalysts of anion-exchange resin and lipase. The whole reaction is depicted as Fig. 1 1 , in which R is m-phenoxybenzyl-. By using enol esters such as vinyl acetate, the reaction becomes irreversible with the yield of the resolution tending to reach 100%. Furthermore, the racemization of the product is greatly reduced when the hydroxyl group of cyanohydrin is protected by acylation. With quinidine used as a base catalyst to catalyze the reaction between m-PBA and AC, the yield of (S)-CPB acetate was only 20%, with the enantio excess (e.e.) being 83% (Inagaki et al., 1992a 1992a ). Use of anion-exchange resin (AmberliteIRA-904) as a base catalyst for the same reaction greatly increased the yield of (S)-CPB acetate to 80%, while the e.e. is relatively unchanged (89%). Although the conversion of the reactant was as high as 80%, the reaction time was as long as 69.6 h (Inagaki et al., 1992b 1992b ). Our group (Zhu et al., 1998 1998 ) compared the different effects of different kinds of lipases, acylating agents (vinyl acetate and isopropenyl acetate) and resins (D301 and D296) on this reaction. Although the reaction time was as long as 24 h, the conversion degree of the reaction was smaller than 17%. Later, a more effective lipase catalyzing the transesterification was screened and the effects of solvent, temperature, reactant concentration and internal and external diffusion limitation on the lipase-catalyzed transesterification were studied (Zhang et al., 2002 2002 ). To our knowledge, there are few published reports on the influence of technological conditions on the whole one-pot synthesis of (S)-CPB acetate in organic media. Optimization of technological conditions in the synthesis of (S)-CPB acetate is discussed in this paper. EXPERIMENTAL DETAILS 1 Chemicals and catalysts 2 Analytically pure grade vinyl acetate, diisopropyl ether, cyclohexane, n-hexadecane, m-PBA were all obtained from Shanghai Biochemical Reagent Corporation (China). Optically pure grade shift reagents Eu(hfc) 3 and CDCl 3 (containing 0.03% tetramethyl silicane (TMS)) were obtained from Sigma Corporation (USA). CPB acetate used for coefficient calibration was prepared by the following protocol: Accurately weighed CPB alcohol (32%) 104.5 g, pyridine 26.3 g and cyclohexane 100 ml were added into a flask placed in a −5 °C ice bath and stirred. Weigh 17 g chloracetate and then put it into a titrating tube. The titration velocity of chloracetate should be appropriately adjusted and the titration reaction should be accompanied by stirring. Switch off the ice machine 1 h after completion of the reaction and switch off the stirrer machine 2 h after the ice bath machine is stopped. Filter the pyridine salt and distill the cyclohexane by vacuum distillation. The lipase separated and purified from Alcaligenes sp. was immobilized and supplied by Meito Sangyo Corporation (Japan). The D301 which is a macroporous, weak base anion-exchange resin, was supplied by Hangzhou Zhengguang Chemical Factory (China). Instruments 2 The instruments and apparatus used in the study are listed in Table 1 1 . Name Type Supplier Isothermal shaker THZ-82A Shanghai Yuejing Medical Instruments Factory, China Electronic balance MD200-3 Shanghai Balance Factory, China Gas chromatograph GC-9790 Zhejiang Wenlin Analytical Instruments Factory, China Chromatographic work station N2000 Institute of Intelligence & Information Engineering of Zhejiang University, China NMR spectrometer DMX500 Bruker Spectrospin Corporation, Switzerland Automatic polarimeter WZZ-2 Shanghai Physical Optics Instruments Factory, China Method to keep the water content stable 2 The immobilized lipase was put into a saturated LiCl solution container kept in a refrigerator at 4 °C for at least 48 h before the use so that the relative moisture was constant (11%). The reproducibility in regard to the reaction rate of lipase-catalyzed reaction was very high, so long as the experiments followed the procedure described by Halling ( 1994 1994 ). Analytical method 2 The samples were analyzed with gas chromatograph with 30 m long capillary (SE30), FID detector with temperature of 280 °C and nitrogen as the carrier gas. The oven temperature was programmed from 80 °C to 200 °C at rate of 20 °C/min and 200 °C to 270 °C at rate of 10 °C/min. The injector temperature was set to 320 °C. Internal standard method was chosen as quantitative analytical method and hexadecane was chosen as the internal standard compound. The calibration coefficient of product CPB acetate was determined to be 2.634. The repeatability was satisfactory. Measurement of e.e. value of CPB acetate by NMR method 2 A sample (ca. 20 mg) was dissolved in a CDCl 3 -TMS (0.03%, V / V ) solution (total 0.5 ml), into which Eu(hfc) 3 (ca. 50 mg) was added. Two signals appeared, δ (chemical shift) 2.31 for (R)-isomer and δ 2.27 for (S)-isomer. Comparison of the integration of these two signals enabled the precise determination of the e.e. General methods for kinetic study 2 The reaction was carried out in a batch reactor (55 ml vial). The reactants (AC, m-PBA, vinyl acetate) and the lipase were weighed accurately. The reaction was started by the addition of the resin D301. In the reaction course, the reactor was placed in a shaker whose rotational speed was controllable and temperature was kept constant. A 0.05 μl of the well-stirred reaction mixture was taken at intervals. The concentrations of CPB acetates were measured by gas chromatograph. Water activity of the solution was kept at 0.01 with definite amount of molecular sieve (Valivety et al., 1992 1992 ). RESULTS AND DISCUSSIONS 1 Choice of solvents 2 The enantioselectivity of the enzyme-catalyzed reaction and the reaction rate in nonaqueous media greatly depended on the solvents (Carrea and Riva, 2000 2000 ; Klibanov, 2001 2001 ). Three solvents were compared in this reaction system. Under the experimental condition (45 °C,220 r/min, the lipase 2.5 mg/ml, D301 5 mg/ml, initial m-PBA concentration 70 mmol/L, initial AC concentration 258 mmol/L), progress curves for the three solvents (vinyl acetate, diisopropyl ether, cyclohexane) were measured. In a preliminary experiment, these three solvents had almost the same solubility of substrates, m-PBA and AC. The effect of the three solvents on enzyme deactivation could be ignored in the reaction time period. The results are shown in Fig. 2 2 . Fig. 2 2 showed that cyclohexane is the first choice to obtain more product in the shortest time, and that diisopropyl ether could make do with the second best. This test just showed the importance of variety of solvent in affecting the degree of conversion of this reaction system. More work should be done to search for the better solvent. C p : Concentration of product; S A0 : Initial concentration of reactant m-PBA; S B0 : Initial concentration of reactant cyanohydrin Effect of temperature 2 It was widely believed that enzymes exhibit their highest stereoselectivity at low temperatures (Phillips, 1996 1996 ). This belief was supported by some experimental observations. In our temperature test, the one-pot reaction was performed under the following conditions: 220 r/min, initial m-PBA concentration 70 mmol/L, initial AC concentration 276 mmol/L, the lipase 2.5 mg/ml, D301 5 mg/ml, vinyl acetate acting as both acyl donor and solvent. In this reaction system, there existed two catalysts–D301 and lipase. The temperature effect on the system must have resulted from the comprehensive influence of the two catalysts. The progress curves of the reaction at different temperatures are shown in Fig. 3 3 and the initial rates, degree of conversion and e.e. values were given in Table 2 2 . T (°C) V 0 ×10 5 mol/(L·s) e.e. (%) Degree of conversion at 1330 min (%) 35 0.031 88.2 7.4 40 0.036 82.5 13.4 45 0.039 65.0 14.2 50 0.046 50.0 24.6 55 0.098 40.2 37.5 Fig. 3 3 and Table 2 2 showed that 55 °C was the optimal temperature for higher degree of conversion. However, the e.e. values of the product decreased gradually with increased reaction temperature. This showed that the enantioselectivity of the lipase decreased with increased temperature, and e.e. value was found to be in negative correlation to degree of conversion in this reaction system. Effect of internal and external diffusion 2 Due to the insolubility of enzyme and D301 in organic media, external diffusion limitation must exist in this reaction system. Furthermore, since the Alcaligenes lipase was an immobilized enzyme, the reactants must first diffuse from the surface of the enzyme to the inner parts of the enzyme and they could then be transformed to products. Therefore, internal diffusion limitation is also existent. Effects of rotational speed and enzyme concentrations on the reaction when the reactant concentration was high enough were studied to reveal the effects of the external and internal diffusion limitations. The effect of rotational speed on the reaction was shown in Fig. 4 4 and Table 3 3 . Rotational speed (r/min) Initial rate [mmol/(L·min)] 110 0.011 155 0.015 190 0.019 220 0.024 240 0.024 260 0.024 Fig. 4 4 showed that the reaction rate increased at rotational speed of 110 r/min to 220 r/min and was almost unchanged at rotational speed higher than 220 r/min (the three curves covered each other). Thus, the conclusion that the external diffusion could be excluded when the rotational speed was higher than 220 r/min could be reasonably drawn. Under the experimental conditions (45 °C, 220 r/min, S A0 =70 mmol/L, S B0 =276 mmol/L), the progress curves of the reaction in different enzyme concentrations were measured (Fig. 5 5 ). The reaction rate increased with increased enzyme concentration (Fig. 5 5 ). The initial rates of each progress curve were calculated and a V 0 (initial reaction rate, mol/(L·s)) vs E 0 (initial enzyme concentration, mol/L) curve was drawn (Fig. 6 6 ). Fig. 6 6 showed that V 0 is not linearly correlated with E 0 . This suggested that the internal diffusion limitation exist in this system (Bedell et al., 1998 1998 ). Effect of reactant concentrations 2 Under the reaction condition (45 °C, 220 r/min, D301 5 mg/ml, lipase 25 mg/ml, vinyl acetate as acyl donor and solvent), the effect of m-PBA concentration (AC concentration was designed to be double of m-PBA) on the one-pot reaction system had been studied. Each progress curve at different m-PBA concentrations was shown in Fig. 7 7 . Fig. 7 7 showed that the reaction rate increased when the initial m-PBA concentration increased from 70 mmol/L to 249 mmol/L but decreased when the m-PBA concentration reached to 277 mmol/L. This implied that substrate inhibition may exist in this reaction system though reduced reaction rate at high substrate concentrations in immobilized enzyme system may also be due to a reaction limited process. The initial rate, degree of conversion and e.e. values were given in Table 4 4 . Degree of conversion at 1840 min decreased when initial m-PBA concentration reached 277 mmol/L. However, change of e.e. had no regularity with the increasing of m-PBA concentration. This reactant concentration test is important and useful for further kinetic study of this reaction. S A0 (mmol/L) Initial rate [mmol/(L·min)] Degree of conversions at 1840 min (%) e.e. (%) 70 0.028 23.2 63.3 126 0.032 22.3 73.3 189 0.051 24.1 55.6 224 0.088 22.3 82.5 249 0.143 22.5 – 277 0.116 17.8 – Comparison of unused lipase and reused lipase 2 Lipase is a relatively expensive catalyst. One of the advantages of synthesis in organic solvent is the convenient recovery of catalyst. In order to check the inactivation rate of lipase in this one-pot reaction system, the catalytic ability of unused lipase and reused lipase was compared (Fig. 8 8 ). It was shown that the catalytic efficiency of new lipase was slightly better than that of the reused lipase. Lipase in organic media could be used for at least more than once or even several times. Optimization of the mole ratio of the two reactants:AC and m-PBA 2 Since there were two reactants, AC and m-PBA in this one-pot reaction system, the mole ratio of the two reactants might be important for obtaining high degree of conversion. In order to determine such effect, we chose five ratios, 0.5:1, 1:1, 1.5:1, 2:1, 3:1 for testing. The reaction degrees of conversions of the five ratios are shown in Table 5 5 . Ratio 2:1 (AC:m-PBA) is shown to be the best choice. Mole ratio of AC to m-PBA Conversions at 1500 min (%) 0.5:1 2.5 1:1 4.8 1.5:1 10.3 2:1 21.5 3:1 19.1 Therefore, it is important to choose an appropriate mole ratio of the two reactants in industrial production in order to get higher conversion. Effect of addition strategy of catalyst D301 2 Under reaction condition (45 °C, 220 r/min, lipase 20 mg, vinyl acetate as solvent 30 ml, S A0 =120 mmol/L, S B0 =240 mmol/L), 0.7 g D301 was added into the system at the beginning of the reaction. The degree of conversion of m-PBA was only 20% at 2500 min. Later, the addition strategy of D301 was changed to adding D301 0.3 g at the beginning of the reaction and then adding D301 0.2 g every 12 h for two times. Surprisingly, the degree of conversion reached 66% at 1500 min, and even as high as 80% at 2500 min (Fig. 9 9 ). We repeated the experiment again, and found that the result was almost the same. The e.e. value of the product measured by NMR was 64.5%. This showed that the base catalyst D301 was easily inactivated in organic solvent, and the addition strategy of D301 is important for getting higher degree of conversion. This result is useful in industrial application. CONCLUSION 1 The one-pot reaction catalyzed by the combination of anion-exchange resin D301 with lipase to synthesize CPB acetate in organic media was studied. By using lipase from Alcaligenes sp., the catalyzing efficiency was improved considerably compared to methods previously reported. Effects of solvents and temperatures on this reaction were studied. External diffusion limitation could be prevented by raising the rotational speed to 220 r/min. In contrast, internal diffusion could not be ignored, since the diameter of the immobilized lipase was not made small enough. The reaction rate was substantially accelerated with the increase of the reactant (m-PBA) concentration to 249 mmol/L, but decreased when the initial concentration of m-PBA was higher than 277 mmol/L. It was also found that the catalyzing capability of recovered lipase was high enough for use in several batches. Finally, the mole ratio of AC to m-PBA and addition strategy of base catalyst D301 to improve the conversion of substrates were studied. By using adequate amount of lipase (0.66 mg/L), adequate amount of D301 (23.33 mg/L) and appropriate addition strategy, the conversion of this one-pot reaction could be as high as 80% even when the temperature was 45 °C, and initial concentration of m-CPB was only 120 mmol/L. The e.e. values of the product decreased gradually when the reaction temperature was raised. This showed that the enantioselectivity of the lipase decreased when the temperature increased. 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Lipase-catalyzed enantioselective transesterification of cyanohydrins for the synthesis of (S)-α-cyano-3-phenoxybenzyl acetate 10.1631/jzus.2005.B0175 Project supported by the National Natural Science Foundation of China (No. 20336010) and the National Basic Research Program (973) of China (No. 2003CB716008) 2004-02-02 2004-09-20 2005-02-20 2022-01-05 Copyright © 2005, Journal of Zhejiang University Science 2005 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 03 6B