SYNTHESIS OF (Z)-3-HEXEN-1-YL BUTYRATE IN HEXANE AND SOLVENT-FREE MEDIUM USING MYCOR MIEHEI AND CANDIDA-ANTARCTICA LIPASES

Citation
S. Bourggarros et al., SYNTHESIS OF (Z)-3-HEXEN-1-YL BUTYRATE IN HEXANE AND SOLVENT-FREE MEDIUM USING MYCOR MIEHEI AND CANDIDA-ANTARCTICA LIPASES, Journal of the American Oil Chemists' Society, 74(11), 1997, pp. 1471-1475
Citations number
35
Categorie Soggetti
Food Science & Tenology","Chemistry Applied
ISSN journal
0003021X
Volume
74
Issue
11
Year of publication
1997
Pages
1471 - 1475
Database
ISI
SICI code
0003-021X(1997)74:11<1471:SO(BIH>2.0.ZU;2-W
Abstract
(Z)-3-Hexen-1-yl butyrate is an important flavor and fragrance compoun d as it represents the model of a natural herbaceous (green) note. Two immobilized lipases from Mucor miehei (Lipozym IM) and from Candida a ntarctica (Novozym 435) were investigated for their use in the synthes is of (Z)-3-hexen-1-yl butyrate by direct esterification in n-hexane. To determine optimal conditions for esterification, we examined the fo llowing parameters: temperature, amount of lipase, acid/alcohol ratio, and absence of solvent. In n-hexane, bioconversion yields reached 95 (after 4 h) and 92% (after 6 h) for, respectively, Lipozym IM [17 (w/w reactants)] and Novozym 435 [2% (w/w reactants)]. In the absence of s olvent, at 60 degrees C, Novozym 435-catalyzed esterification afforded the title compound in 80% yield. Up to 250 g (in hexane) and 160 g (w ithout solvent) of ester were easily prepared, in a single operation, at a laboratory scale, in few hours, using 2% (w/w reactants) lipase.