Esterification of hydroxy compounds by fatty acid anhydrides

Partial glycerides are rapidly and completely esterified at room temperature to triglycerides by fatty acid anhydrides in the presence of perchloric acid. This esterification occurs without isomerization of the partial glyceride. As a consequence, by the use of partial glycerides of the appropriate...

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Main Authors: F.H. Mattson, R.A. Volpenhein, James B. Martin
Format: Article
Language:English
Published: Elsevier 1964-07-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520402081
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spelling doaj-321cde7a32f34bc8833e8e76ed9831a82021-04-23T06:12:13ZengElsevierJournal of Lipid Research0022-22751964-07-0153374377Esterification of hydroxy compounds by fatty acid anhydridesF.H. Mattson0R.A. Volpenhein1James B. Martin2The Procter & Gamble Company, Miami Valley Laboratories, Cincinnati, OhioThe Procter & Gamble Company, Miami Valley Laboratories, Cincinnati, OhioThe Procter & Gamble Company, Miami Valley Laboratories, Cincinnati, OhioPartial glycerides are rapidly and completely esterified at room temperature to triglycerides by fatty acid anhydrides in the presence of perchloric acid. This esterification occurs without isomerization of the partial glyceride. As a consequence, by the use of partial glycerides of the appropriate structure, triglycerides having a specific structure can be prepared by this means. Other strong acids also catalyze esterification at room temperature, but this is accompanied by isomerization of the partial glyceride. The effect of varying the reaction conditions on the nature and extent of the reaction with partial glycerides has been determined. Alcohols also can be esterified by fatty acid anhydrides in the presence of perchloric acid.http://www.sciencedirect.com/science/article/pii/S0022227520402081
collection DOAJ
language English
format Article
sources DOAJ
author F.H. Mattson
R.A. Volpenhein
James B. Martin
spellingShingle F.H. Mattson
R.A. Volpenhein
James B. Martin
Esterification of hydroxy compounds by fatty acid anhydrides
Journal of Lipid Research
author_facet F.H. Mattson
R.A. Volpenhein
James B. Martin
author_sort F.H. Mattson
title Esterification of hydroxy compounds by fatty acid anhydrides
title_short Esterification of hydroxy compounds by fatty acid anhydrides
title_full Esterification of hydroxy compounds by fatty acid anhydrides
title_fullStr Esterification of hydroxy compounds by fatty acid anhydrides
title_full_unstemmed Esterification of hydroxy compounds by fatty acid anhydrides
title_sort esterification of hydroxy compounds by fatty acid anhydrides
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1964-07-01
description Partial glycerides are rapidly and completely esterified at room temperature to triglycerides by fatty acid anhydrides in the presence of perchloric acid. This esterification occurs without isomerization of the partial glyceride. As a consequence, by the use of partial glycerides of the appropriate structure, triglycerides having a specific structure can be prepared by this means. Other strong acids also catalyze esterification at room temperature, but this is accompanied by isomerization of the partial glyceride. The effect of varying the reaction conditions on the nature and extent of the reaction with partial glycerides has been determined. Alcohols also can be esterified by fatty acid anhydrides in the presence of perchloric acid.
url http://www.sciencedirect.com/science/article/pii/S0022227520402081
work_keys_str_mv AT fhmattson esterificationofhydroxycompoundsbyfattyacidanhydrides
AT ravolpenhein esterificationofhydroxycompoundsbyfattyacidanhydrides
AT jamesbmartin esterificationofhydroxycompoundsbyfattyacidanhydrides
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