Conclusions
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1.
It has been shown that conditions for the liquid-phase catalytic reduction of aromatic nitro compounds have a different effect on the hydrogenation of the nitro compounds to the corresponding arylhydroxylamine and on the disproportionation of the latter with the formation of amines.
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2.
Contrary to the hydrogenation of the nitro group, the disproportionation rate of the arylhydroxylamines depends to a large degree on the temperature and the pH of the medium. Electron-donor substituents increase the disproportionation rate, while electron-acceptor substituents reduce it.
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3.
The conditions have been determined at which an increased yield of arylhydroxy1amines is obtained in the catalytic reduction of the nitro compounds.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 760–764, April, 1983.
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Makaryan, I.A., Savchenko, V.I. & Brikenshtein, K.A. Influence of process conditions on the kinetics of the liquid-phase catalytic hydrogenation of aromatic nitro compounds. Russ Chem Bull 32, 692–695 (1983). https://doi.org/10.1007/BF00953458
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DOI: https://doi.org/10.1007/BF00953458