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Polymer precursors from catalytic reactions of natural oils†
Marc R. L. Furst,Ronan Le Goff,Dorothee Quinzler,Stefan Mecking,Catherine H. Botting,David J. Cole-Hamilton
Green Chemistry Pub Date : 12/14/2011 00:00:00 , DOI:10.1039/C1GC16094J
Abstract

Dimethyl 1,19-nonadecanedioate is produced from the methoxycarbonylation of commercial olive, rapeseed or sunflower oils in the presence of a catalyst derived from [Pd2(dba)3], bis(ditertiarybutylphosphinomethyl)benzene (BDTBPMB) and methanesulphonic acid (MSA). The diester is then hydrogenated to 1,19-nonadecanediol using Ru/1,1,1-tris-(diphenylphosphinemethyl)ethane (triphos). 1,19-Nonadecadienoic acid is hydrogenated to short chain oligoesters, which can themselves be hydrogenated to 1,19-nonadecanol by hydrogenation in the presence of water.

Graphical abstract: Polymer precursors from catalytic reactions of natural oils
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