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Condensation of dicyandiamide with chloral hydrate

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A substituted 1,3,5-oxadiazine derivative that exists in two tautomeric forms was obtained by reaction of dicyandiamide with chloral hydrate. The structure of the product was established on the basis of its IR spectrum and chemical transformations.

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Literature cited

  1. A. E. Kretov and G. V. Tikhonov, Zh. Obshch. Khim., 34, 2429 (1964).

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  2. N. N. Mel'nikov, Yu. A. Beskakov, and M. E. Kuperman, Organic Insectofungicides and Herbicides [in Russian], Goskhimizdat, Moscow (1958), p. 266.

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Authors and Affiliations

  1. Armenian Agricultural Institute, Erevan

    V. V. Dovlatyan, T. Z. Papoyan & G. K. Tarkhanyan

Authors
  1. V. V. Dovlatyan
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  2. T. Z. Papoyan
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  3. G. K. Tarkhanyan
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 473–474, April, 1975.

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Dovlatyan, V.V., Papoyan, T.Z. & Tarkhanyan, G.K. Condensation of dicyandiamide with chloral hydrate. Chem Heterocycl Compd 11, 415–416 (1975). https://doi.org/10.1007/BF00502425

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  • DOI: https://doi.org/10.1007/BF00502425

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