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Oxidation of organic compounds

LI. Synthesis of 2,5-dicyanopyridine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The synthesis of 2, 5-dicyanopyridine from the industrially available 5-ethyl-2-methylpyridine has been effected by oxidative ammonolysis in the presence of a vanadium-tin oxide catalyst and by oxidation with nitric acid to isocinchomeronic acid with the subsequent conversion of the latter into the dichloride, diamide, and dinitrile. The IR spectra of 2, 5-dicyanopyridine have been obtained and its polarographic behavior has been studied.

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References

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Authors and Affiliations

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

    E. A. Pavlov, V. A. Serazetdinova, A. D. Kagarlitskii & B. V. Suvorov

Authors
  1. E. A. Pavlov
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  2. V. A. Serazetdinova
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  3. A. D. Kagarlitskii
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  4. B. V. Suvorov
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Additional information

For part L, see [1].

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Pavlov, E.A., Serazetdinova, V.A., Kagarlitskii, A.D. et al. Oxidation of organic compounds. Chem Heterocycl Compd 4, 488–489 (1971). https://doi.org/10.1007/BF00486766

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  • DOI: https://doi.org/10.1007/BF00486766

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