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Reductive alkylation of p-phenylenediamine and its hydroquinone complex with ketones in presence of rhenium and palladium sulfides
Authors:M. A. Ryashentseva  Kh. M. Minachev  L. S. Geidysh
Affiliation:(1) N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, USSR
Abstract:Conclusions Conditions were found (150–200°, hydrogen pressure 110–150 atm, reaction time 3 h) for the reductive alkylation of p-phenylenediamine and its hydroquinone complex with acetone, butanone, and cyclohexanone in presence of Re2S7 or PdS as catalyst, and N,N'-diisopropyl-, N,N'-di-s-butyl-, and N,N'-dicyclohexyl-p-phenylenediamines and their hydroquinone complexes were obtained in 60–90% yield.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1601–1605, July, 1968.
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