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 |
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Hauptverfasser: | , , , , , , |
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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. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c5ob02376a |