Volume 19, Issue 18
Preparative Organic Chemistry
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ChemInform Abstract: The “ipso” Effect of Silicium in the Acylation of m-Trimethylsilylanisole.

B. BENNETAU

B. BENNETAU

Lab. Chim. Org. Organomet., CNRS, Univ. Bordeaux I, 33405 Talence, France

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M. KREMPP

M. KREMPP

Lab. Chim. Org. Organomet., CNRS, Univ. Bordeaux I, 33405 Talence, France

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J. DUNOGUES

J. DUNOGUES

Lab. Chim. Org. Organomet., CNRS, Univ. Bordeaux I, 33405 Talence, France

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First published: May 3, 1988

Abstract

Acylation of m-trimethylsilylanisole (I) using benzoyl chloride (II) or acetyl chloride (VII) gives the distribution of products as shown in the reaction scheme.

ChemInform Abstract

Acylation of m-trimethylsilylanisole (I) using benzoyl chloride (II) or acetyl chloride (VII) gives the distribution of products as shown in the reaction scheme. This result of the reaction demonstrates clearly that the ipso effect of the trimethylsilyl group is countered by the methoxy group.

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