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Synthesis of ( Z )‐3‐hexen‐1‐yl butyrate in hexane and solvent‐free medium using Mucor miehei and Candida antarctica lipases
Author(s) -
BourgGarros S.,
Razafindramboa N.,
Pavia A. A.
Publication year - 1997
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/s11746-997-0256-0
Subject(s) - candida antarctica , chemistry , solvent , hexane , rhizopus oryzae , lipase , yield (engineering) , organic chemistry , rhizomucor miehei , chromatography , triacylglycerol lipase , fermentation , enzyme , materials science , metallurgy
( Z )‐3‐Hexen‐1‐yl butyrate is an important flavor and fragrance compound as it represents the model of a natural herbaceous (green) note. Two immobilized lipases from Mucor miehei (Lipozym IM) and from Candida antarctica (Novozym 435) were investigated for their use in the synthesis of ( Z )‐3‐hexen‐1‐yl butyrate by direct esterification in n ‐hexane. To determine optimal conditions for esterification, we examined the following 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 solvent, at 60°C, Novozym 435‐catalyzed esterification afforded the title compound in 80% yield. Up to 250 g (in hexane) and 160 g (without solvent) of ester were easily prepared, in a single operation, at a laboratory scale, in few hours, using 2% (w/w reactants) lipase.