Issue 14, 2000
From the journal:

Chemical Communications

Acylation of activated aromatics without added acid catalyst

James S. Brown,a   Roger Gläser,a   Charles L. Liottaa  and  Charles A. Eckert*a  

* Corresponding authors

a Schools of Chemical Engineering, Chemistry and Biochemistry, and Specialty Separations Center, Georgia Institute of Technology, Atlanta, USA.
E-mail: cae@che.gatech.edu

Abstract

Phenol and resorcinol can be acetylated to the corresponding esters and ketones in aqueous and neat acetic acid at high temperature (250–300 °C) to substantial equilibrium conversion without any added acid catalyst.

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Article information

DOI
https://doi.org/10.1039/B001544J
Article type
Communication
Submitted
24 Feb 2000
Accepted
15 May 2000
First published
26 Jun 2000

Chem. Commun., 2000, 1295-1296

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Acylation of activated aromatics without added acid catalyst

J. S. Brown, R. Gläser, C. L. Liotta and C. A. Eckert, Chem. Commun., 2000, 1295 DOI: 10.1039/B001544J

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