Lipase-Catalyzed Transesterification of (R,S)-1-Phenylethanol in SC CO2 and in SC CO2/Ionic Liquid Systems

被引:0
作者
Paljevac, Muzafera [1 ]
Knez, Zeljko [1 ]
Habulin, Maja [1 ]
机构
[1] Univ Maribor, Fac Chem & Chem Engn, Lab Separat Proc & Prod Design, SI-2000 Maribor, Slovenia
关键词
Candida antarctica lipase B; transesterification; (R; S)-1-phenylethanol; vinyl acetate; supercritical carbon dioxide; ionic liquids; CANDIDA-ANTARCTICA LIPASE; SUPERCRITICAL CARBON-DIOXIDE; IONIC LIQUIDS; KINETIC RESOLUTION; ENZYMATIC-SYNTHESIS; IMMOBILIZED LIPASE; WATER ACTIVITY; CHAIN-LENGTH; BIOCATALYSIS; ENANTIOSELECTIVITY;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Commercial immobilized lipase B from Candida antarctica (CALB) was successfully applied to catalyzing the transesterification of (R,S)-1-phenylethanol in supercritical carbon dioxide and in supercritical carbon dioxide/ionic liquid biphasic system. Firstly, the variables affecting the performance of CALB in transesterification reactions in supercritical carbon dioxide, such as CALB concentration, temperature and pressure, were studied. An increase in the conversion and in the reaction rate was observed as the CALB/substrate ratio, temperature and pressure, were increased from 4.3 to 19.9, from 40 degrees C to 80 degrees C and from 8 MPa to 10 MPa, respectively. Further increase in temperature from 80 degrees C to 120 degrees C and pressure from 10 MPa to 30 MPa resulted in lower conversion and lower initial reaction rate. Furthermore, different vinyl esters were used as acyl donors for CALB-catalyzed transesterification of (R,S)-1-phenylethanol in supercritical carbon dioxide. The highest initial reaction rate was attained with vinyl butyrate, although 50% conversion was attained faster when vinyl acetate was used as acyl donor. Secondly, in transesterification of (R,S)-1-phenylethanol, performed in supercritical carbon dioxide/ionic liquid biphasic system, influence of concentration of 1-butyl-3-methylimidazolium tetrafluoroborate [bmim][BF4] was studied. The addition of 50 mmol (70% w/w reaction mixture) of [bmim][BF4] to the reaction system gave the best result in terms of transesterification rate.
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页码:815 / 825
页数:11
相关论文
共 53 条
[1]  
Aaltonen O., 1999, CHEM SYNTHESIS USING, P414, DOI [DOI 10.1002/9783527613687, 10.1002/9783527613687]
[2]   Novozym 435 activity in compressed gases. Water activity and temperature effects [J].
Almeida, MC ;
Ruivo, R ;
Maia, C ;
Freire, L ;
de Sampaio, TC ;
Barreiros, S .
ENZYME AND MICROBIAL TECHNOLOGY, 1998, 22 (06) :494-499
[3]  
Bailey JE., 1986, BIOCH ENG FUNDAMENTA, V2nd
[4]   Highly enantioselective aminoacylase-catalyzed transesterification of secondary alcohols [J].
Bakker, M ;
Spruijt, AS ;
van Rantwijk, F ;
Sheldon, RA .
TETRAHEDRON-ASYMMETRY, 2000, 11 (08) :1801-1808
[5]   Supercritical and near-critical CO2 in green chemical synthesis and processing [J].
Beckman, EJ .
JOURNAL OF SUPERCRITICAL FLUIDS, 2004, 28 (2-3) :121-191
[6]   Recovery of organic products from ionic liquids using supercritical carbon dioxide [J].
Blanchard, LA ;
Brennecke, JF .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2001, 40 (01) :287-292
[7]   Green processing using ionic liquids and CO2 [J].
Blanchard, LA ;
Hancu, D ;
Beckman, EJ ;
Brennecke, JF .
NATURE, 1999, 399 (6731) :28-29
[8]   Lipase-catalyzed solid phase synthesis of sugar fatty acid esters [J].
Cao, LQ ;
Fischer, A ;
Bornscheuer, UT ;
Schmid, RD .
BIOCATALYSIS AND BIOTRANSFORMATION, 1997, 14 (04) :269-283
[9]   Stability and stabilization of hydroxynitrile lyase in organic solvents [J].
Costes, D ;
Rotcenkovs, G ;
Wehtje, E ;
Adlercreutz, P .
BIOCATALYSIS AND BIOTRANSFORMATION, 2001, 19 (02) :119-130
[10]   A STRUCTURAL BASIS FOR THE CHIRAL PREFERENCES OF LIPASES [J].
CYGLER, M ;
GROCHULSKI, P ;
KAZLAUSKAS, RJ ;
SCHRAG, JD ;
BOUTHILLIER, F ;
RUBIN, B ;
SERREQI, AN ;
GUPTA, AK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (08) :3180-3186