Base-induced alcoholysis of N-arylmaleimides: Facile in situ oxa-michael addition to alkyl maleanilates: Two-step one-pot rapid access to alkoxysuccinic acids

摘要

A simple, efficient and general two-step, one-pot approach to alkoxysuccinic acids is described. The potassium carbonate-catalyzed reactions of alcohols with N-p-tolylmaleimide (4) followed by an acid-induced hydrolysis of intermediate products furnished alkoxysuccinic acids 1a-f in 90-98% yields. All the intermediates from the reaction of imide 4 with alcohols have been isolated and characterized, proving that the in situ formed alkyl maleanilates 3 are the actual Michael acceptors. [References: 60]