Publication | Closed Access
Copper-Catalyzed One-Pot Synthesis of 1,2,4-Triazoles from Nitriles and Hydroxylamine
65
Citations
34
References
2015
Year
Novel OrganocatalystsEngineeringCopper-catalyzed One-pot Synthesis1,2,4-Triazole DerivativesOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistrySynthesis MethodAvailable NitrilesSubstituted 1,2,4-TriazolesSynthetic Chemistry
A simple and efficient copper-catalyzed one-pot synthesis of substituted 1,2,4-triazoles through reactions of two nitriles with hydroxylamine has been developed. The protocol uses simple and readily available nitriles and hydroxylamine hydrochloride as the starting materials and inexpensive Cu(OAc)2 as the catalyst, and the corresponding 1,2,4-triazole derivatives are obtained in moderate to good yields. The reactions include sequential intermolecular addition of hydroxylamine to one nitrile to provide amidoxime, copper-catalyzed treatment of the amidoxime with another nitrile, and intramolecular dehydration/cyclization. This finding provides a new and useful strategy for synthesis of 1,2,4-triazole derivatives.
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