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Synthesis of 3,5-dicya nopyridine by oxidative ammonolysis of 3,5-lutidine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Pyridine-3,5-dicarboxylic acid was synthesized by oxidative ammonolysis of 3,5-lutidine and hydrolysis of the resulting 3,5-dicyanopyridine.

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Literature cited

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Authors and Affiliations

  1. Institute of Chemical Sciences, Academy of Sciences of the Kazakh SSR, Alma-Ata.

    B. V. Suvorov, A. D. Kagarlitskii, N. A. Belova & R. T. Kutzhanov

Authors
  1. B. V. Suvorov
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  2. A. D. Kagarlitskii
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  3. N. A. Belova
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  4. R. T. Kutzhanov
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Additional information

Communication XCIV from the series “Oxidation of Organic Compounds”; see [1] for communication XCIII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 819–820, June, 1973.

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Suvorov, B.V., Kagarlitskii, A.D., Belova, N.A. et al. Synthesis of 3,5-dicya nopyridine by oxidative ammonolysis of 3,5-lutidine. Chem Heterocycl Compd 9, 751–752 (1973). https://doi.org/10.1007/BF00472324

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  • DOI: https://doi.org/10.1007/BF00472324

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