Reductive alkylation of p-phenylenediamine and its hydroquinone complex with ketones in presence of rhenium and palladium sulfides |
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Authors: | M. A. Ryashentseva Kh. M. Minachev L. S. Geidysh |
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Affiliation: | (1) N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, USSR |
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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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