ChemInform Abstract: Diprotodecarboxylation Reactions of 3,4‐Dialkoxythiophene‐2,5‐dicarboxylic Acids Mediated by Ag2CO3 and Microwaves.

Abstract

Abstract An efficient and rapid method is reported to obtain 3,4-dialkoxythiophenes from 3,4-dialkoxythiophene-2,5-dicarboxylic acids through a diprotodecarboxylation reaction with Ag2CO3/AcOH as a catalytic system and microwave heating in dimethylsulfoxide (DMSO) as solvent. This methodology lets us obtain for the first time good performance with thiophenes bearing strong electron-donating groups such as alkoxides. This methodology eliminates the usage of harmful quinoline as solvent, as well as the long reaction times typically used (12–18 h) to obtain the 3,4-dialkoxythiophenes. The reaction of 7 diacids showed good yields (60–89%) following 20 min of microwave heating in a temperature range of 120–150 °C. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.]