Issue 2, 2017

Highly selective biocatalytic synthesis of monoacylglycerides in sponge-like ionic liquids

Abstract

The biocatalytic synthesis of monoacylglycerides (MAGs) was carried out by the direct esterification of fatty acids (i.e. capric, lauric, myristic, palmitic and oleic acids, respectively) with glycerol in different ionic liquids (ILs) based on cations with long alkyl side-chains (e.g. 1-hexadecyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide [C16mim][NTf2], 1-dodecyl-3-methylimidazolium tetrafluoroborate [C12mim][BF4], etc.). Although all ILs have been shown as suitable reaction media for Novozym 435-catalyzed esterification of glycerol with free fatty acids, a high selectivity of MAGs was only observed in the [C12mim][BF4] case (e.g. up to 100% selectivity and 100% yield for monolaurin). Furthermore, as these ILs are temperature switchable ionic liquid/solid phases that behave as sponge-like systems, a straightforward protocol for IL-free MAG recovery, based on iterative centrifugations at controlled temperature, has been developed.

Graphical abstract: Highly selective biocatalytic synthesis of monoacylglycerides in sponge-like ionic liquids

Supplementary files

Article information

Article type
Paper
Submitted
19 7 2016
Accepted
24 8 2016
First published
25 8 2016

Green Chem., 2017,19, 390-396

Highly selective biocatalytic synthesis of monoacylglycerides in sponge-like ionic liquids

P. Lozano, C. Gomez, S. Nieto, G. Sanchez-Gomez, E. García-Verdugo and S. V. Luis, Green Chem., 2017, 19, 390 DOI: 10.1039/C6GC01969B

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