Colloid and nanosized catalysts in organic synthesis: XIV. Reductive amination and amidation of carbonitriles catalyzed by nickel nanoparticles


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Abstract

Hydrogenation of carbonitriles catalyzed by nickel nanoparticles in the presence of primary amines led to the predominant formation of unsymmetrical secondary amines. In the presence of secondary amines hydrogenation of nitrites provided enamines as main products. Hydrogenation of nitriles in the presence of formamide or acetamide afforded formyl or acetyl derivatives of primary amines.

About the authors

Yu. V. Popov

Volgograd State Technical University

Author for correspondence.
Email: tons@vstu.ru
Russian Federation, pr. Lenina 28, Volgograd, 400131

V. M. Mokhov

Volgograd State Technical University

Email: tons@vstu.ru
Russian Federation, pr. Lenina 28, Volgograd, 400131

K. V. Shcherbakova

Volgograd State Technical University

Email: tons@vstu.ru
Russian Federation, pr. Lenina 28, Volgograd, 400131


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