Direct oxidative amidation of aldehydes with amines catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions a dual-catalysis process

A simple and efficient procedure for the synthesis of amides directly from aldehydes and amines catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions has been reported. The practical protocol was found to tolerate a wide range of substrates with different functional groups....

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Veröffentlicht in:Organic & biomolecular chemistry 2016-01, Vol.14 (5), p.1784-1793
Hauptverfasser: Fu, Renzhong, Yang, Yang, Zhang, Jin, Shao, Jintao, Xia, Xuming, Ma, Yunsheng, Yuan, Rongxin
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Zusammenfassung:A simple and efficient procedure for the synthesis of amides directly from aldehydes and amines catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions has been reported. The practical protocol was found to tolerate a wide range of substrates with different functional groups. Moderate to excellent yields, solvent-free media, and operational simplicity are the main highlights. The proposed dual-catalysis mechanistic pathway was briefly investigated. Furthermore, the heteropolyanion-based ionic liquids were easily reusable for this oxidative amidation. A heteropolyanion-based ionic liquid catalyzed oxidative amidation of aldehydes with amines via a dual-catalysis pathway has been reported.
ISSN:1477-0520
1477-0539
DOI:10.1039/c5ob02376a