Hydrogenation of aromatic nitro compounds on palladium-containing anion-exchange resins


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Abstract

Hydrogenation of aromatic nitro compounds to the corresponding amines on palladium-containing anion-exchange resins has been studied under mild conditions. It has been found that stericity has a significant effect on the activity and selectivity of the hydrogenation reaction. High efficiency of the palladium-containing anion-exchange resins in the synthesis of aromatic amines has been demonstrated. Halonitrobenzenes undergo intense dehalogenation resulting in a low yield of the corresponding amine.

About the authors

M. G. Abdullaev

Dagestan State University

Author for correspondence.
Email: mahram-ivgu@rambler.ru
Russian Federation, ul. Gadzhieva 43a, Makhachkala, Dagestan, 367025

Z. G. Gebekova

lagestan State Pedagogical University

Email: mahram-ivgu@rambler.ru
Russian Federation, ul. Yaragskogo 57, Makhachkala, Dagestan, 367003

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