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
(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.