Issue 58, 2015

Hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes to (N,N-disubstituted aminomethyl)anilines catalyzed by palladium–nickel bimetallic nanoparticles

Abstract

Since palladium-catalysts have strong abilities for both hydrogenation of nitro-group and hydrogenolysis of benzylamine, they have a much lower chemoselectivity for the hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes. In this article, component stable Pd–Ni bimetallic nanoparticles were prepared by simply heating RANEY®-Ni and Na2PdCl4 together in water. They demonstrated novel synergistic effects when they were used as a bimetallic catalyst, by which a highly efficient and chemoselective hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes to (N,N-disubstituted aminomethyl)anilines was achieved.

Graphical abstract: Hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes to (N,N-disubstituted aminomethyl)anilines catalyzed by palladium–nickel bimetallic nanoparticles

Supplementary files

Article information

Article type
Paper
Submitted
21 Apr 2015
Accepted
20 May 2015
First published
20 May 2015

RSC Adv., 2015,5, 47125-47130

Author version available

Hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes to (N,N-disubstituted aminomethyl)anilines catalyzed by palladium–nickel bimetallic nanoparticles

H. Bao, D. Wang, X. Wang, C. Cheng, Y. Li and Y. Hu, RSC Adv., 2015, 5, 47125 DOI: 10.1039/C5RA07208E

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