Propanolysis of esters using chlorotrimethylsilane

Article abstract of DOI:10.1080/00397919908086082

A variety of methyl esters are converted into the corresponding propyl esters upon treatment with 1-propanol and chlorotrimethylsilane. Among them acyclic aliphatic esters have the best conversion rate.

Full text of DOI:10.1080/00397919908086082

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Synthetic Communications: An
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Organic Chemistry
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Propanolysis of Esters Using
Chlorotrimethylsilane
Jordi Eras a , Montserrat Llovera a , Xavier Ferran a b
& Ramon Canela a b
a Chemistry Department (Universitat de Lleida) ,
Rovira Roure, 177, 25198, Lleida, Spain
b Area of Crop Protection, Centre R+D (UdL-IRTA) ,
Rovira Roure, 177, 25198, Lleida, Spain
Published online: 17 Sep 2007.
To cite this article: Jordi Eras , Montserrat Llovera , Xavier Ferran & Ramon Canela
(1999) Propanolysis of Esters Using Chlorotrimethylsilane, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
29:7, 1129-1133, DOI: 10.1080/00397919908086082
To link to this article: http://dx.doi.org/10.1080/00397919908086082
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