Synthesis 2003(3): 0346-0349
DOI: 10.1055/s-2003-37351
PAPER
© Georg Thieme Verlag Stuttgart · New York

Facile Routes to Alkoxymaleimides/Maleic Anhydrides [1]

Manoj Kumar Sahoo, Santosh B. Mhaske, Narshinha P. Argade*
Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune 411 008, India
Fax: +91(20)5893153; e-Mail: argade@dalton.ncl.res.in;
Further Information

Publication History

Received 15 October 2002
Publication Date:
19 February 2003 (online)

Abstract

New routes to alkoxymaleic anhydrides 1a/b have been described in good yields via base-induced chemoselective vinylic substitution of bromo atom in bromomaleimide 4 with alkanols, and base-induced oxa-Micahel addition of alkanols to dialkyl acetylenedicarboxylates 8a/b as key steps. An unusual acyl exchange in the conversion of 6a/b to 1a/b under very simple and mild reaction conditions is noteworthy.

1

NCL Communication No. 6633.

1

NCL Communication No. 6633.

14

Mhaske, S. B.; Argade, N. P., unpublished results.