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Reductive acylation of 5-nitro-2R-thiophenes

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A study was made of the kinetics of the reduction of eleven 5-nitro-2-substituted thiophenes to acetylaminothiophenes using Raney nickel in acetic anhydride. The dependence of the rate of the reaction both on the induction effect of the substituents and on the ratio of the adsorption constants of the reaction products and substrate was determined.

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Authors and Affiliations

  1. All-Union Monomer Scientific-Research and Planning Institute, 300600, Tula

    A. A. Glushkova, L. M. Morgunova, G. N. Freidlin, A. Ya. Fedorov & V. F. Ivanov

Authors
  1. A. A. Glushkova
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  2. L. M. Morgunova
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  3. G. N. Freidlin
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  4. A. Ya. Fedorov
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  5. V. F. Ivanov
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Additional information

Translated from Khimiya Geterosiklicheskikh Soedinenii, No. 4, pp. 455–459, April, 1987.

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Glushkova, A.A., Morgunova, L.M., Freidlin, G.N. et al. Reductive acylation of 5-nitro-2R-thiophenes. Chem Heterocycl Compd 23, 380–384 (1987). https://doi.org/10.1007/BF00546728

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  • DOI: https://doi.org/10.1007/BF00546728

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