A CONVENIENT ACYLATION PROCEDURE OF ALCOH OLS AND AMINES

Citation
Ay. Misharin et Bk. Chernov, A CONVENIENT ACYLATION PROCEDURE OF ALCOH OLS AND AMINES, Bioorganiceskaa himia, 23(8), 1997, pp. 675-679
Citations number
14
Journal title
ISSN journal
01323423
Volume
23
Issue
8
Year of publication
1997
Pages
675 - 679
Database
ISI
SICI code
0132-3423(1997)23:8<675:ACAPOA>2.0.ZU;2-Z
Abstract
The reaction of carboxylic acids with primary and secondary alcohols i n the presence of aromatic sulfochlorides (mesitylenesulfonyl chloride and 2,4,6-triisopropylbenzenesulfonyl chloride) or aromatic sulfotetr azoles (mesytilenesulfonyl tetrazolide and 2,4,6-triisopropylbenzenesu lfonyl tetrazolide) and usual acylation catalysts was shown to be a co nvenient procedure for the synthesis of esters. Reaction of carboxylic acids with primary aliphatic or aromatic amines in the presence of th e same tetrazolides and catalysts is a useful procedure for the synthe sis of amides. Syntheses of twenty compounds are presented as examples .