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Cyclotrimerization of thiocyanic acid in organic solvents

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Thiocyanic acid in organic solvents (i-PrOH Bu2O, AcOH, dioxane) trimerizes to form 1,3,5-trimercapto-sym-triazine.

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Literature Cited

  1. Ch. L. Melamed and G. A. Blok, Kauch. Rezin., No. 8, 10 (1969).

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  2. E. Smolin and L. Rapaport, s-Triazines and Derivatives, Interscience, New York (1959), p. 106.

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  3. H. E. Williams, Cyanogen Compounds, Chemical Publishing Co., New York (1948), p. 261.

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Authors and Affiliations

  1. Dzerzhinskii Branch of the A. A. Zhdanov Gor'kovskii Polytechnical Institute, 606026, Dzerzhinsk

    A. G. Rybin, E. N. Zil'berman, I. V. étlis & G. N. Chervyakova

Authors
  1. A. G. Rybin
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  2. E. N. Zil'berman
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  3. I. V. étlis
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  4. G. N. Chervyakova
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1246–1247, September, 1986.

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Rybin, A.G., Zil'berman, E.N., étlis, I.V. et al. Cyclotrimerization of thiocyanic acid in organic solvents. Chem Heterocycl Compd 22, 1009–1010 (1986). https://doi.org/10.1007/BF00478136

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  • DOI: https://doi.org/10.1007/BF00478136

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