Premium
Fatty acid esters of methylglucoside prepared by the alcoholysis reaction
Author(s) -
Wolff Hans,
Hill W. H.
Publication year - 1948
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/bf02593479
Subject(s) - hydrolysis , chemistry , organic chemistry , fatty acid
SummaryAlcoholysis of triglycerides by methylglucoside gave an impure reaction mixture containing from 60–70% of glucoside‐monoesters. The mono‐, di‐, and trioleoyl methylglucosides were prepared by alcoholysis of methyloleate with α‐methylglucoside. Hydrolysis of the glucoside esters of fatty acids to dextrose esters could not be achieved. The ester linkage hydrolyzed in preference to the acetal linkage.