2-Acyloxy-4,6-dimethoxy-1,3,5-triazine - A New Reagent for Ester Synthesis

Janina E. Kamińska; Zbigniew J. Kamiński; Józef Góra

doi:10.1055/s-1999-3448

Synthesis 1999; 1999(4): 593-596
DOI: 10.1055/s-1999-3448

paper

© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

2-Acyloxy-4,6-dimethoxy-1,3,5-triazine - A New Reagent for Ester Synthesis

Janina E. Kamińska^* , Zbigniew J. Kamiński, Józef Góra

^*Institute of General Food Chemistry, Technical University of Łódź, ul. Stefanowskiego 4/10, 90-924 Łódź, Poland; Fax +48(42)6 36 28 60; E-mail: jekamins@snack.p.lodz.pl

Abstract

als PDF herunterladen Alle Artikel dieser Rubrik

2-Acyloxy-4,6-dimethoxy-1,3,5-triazines obtained in reaction between carboxylic acid and 2-chloro-4,6-dimethoxy-1,3,5-triazine were used as acylating agents for the synthesis of esters from primary, secondary, and tertiary alcohols. Because of mild acylation conditions the method could be applied to esterification of labile alcohols with aromatic and aliphatic (also α-branched) acids in good yields.

transesterification - alcoholysis - catalyst - magnesium bromide

PDF (47 kb)