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A study of the oxidative ammonolysis of quinoline

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The oxidative ammonolysis of quinoline has been studied. The main products are pyridine, benzene, benzonitrile, and nicotinonitrile. Free nicotinic and benzoic acids and their amides are formed in small amounts. The gaseous products of the reaction are hydrogen cyanide and oxides of carbon. The most significant factors determining the direction of the process are the content of tin oxides in the catalysts, the concentration of ammonia in the feed gases, and the temperature of the reaction.

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Literature cited

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Authors and Affiliations

  1. All-Union Scientific-Research Vitamiń Institute, Moscow

    I. B. Chekmareva, E. S. Zhdanovich & B. V. Suvorov

Authors
  1. I. B. Chekmareva
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  2. E. S. Zhdanovich
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  3. B. V. Suvorov
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Translated from Khimiya Geterotsiklicheskikh Soedinii, Vol. 6, No. 6, pp. 794–797, June, 1970.

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Chekmareva, I.B., Zhdanovich, E.S. & Suvorov, B.V. A study of the oxidative ammonolysis of quinoline. Chem Heterocycl Compd 6, 735–738 (1970). https://doi.org/10.1007/BF00470530

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  • DOI: https://doi.org/10.1007/BF00470530

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