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Peculiarities of the chlorination of vinylindole in halogenation reactions

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    We were the first to study the halogenation of vinylindole. Chlorination of the compound yields diindolyl-N, N'-(α,α'-dichloro)butane.

  2. 2.

    The product formed in the first stage of the bromination of vinylindole is 1-(α,β -dibromo)ethylindole, while 1-(α,β,β-tribromo)ethylindole is obtained when excess bromine is used.

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Literature cited

  1. M. F. Shostakovskii and F. P. Sidel'kovskaya, Zh. Obshch. Khim.,21, 1610 (1951).

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  2. M. F. Shostakovskii and A. V. Bogdanova Zh. Obshch. Khim.,17, 565 (1947).

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  3. F. P. Sidel'kovskaya, M. G. Zelenskaya, and M. F. Shostakovskii, Izv. AN SSSR, Otd. Khim. Nauk,1958, 1111.

  4. M. F. Shostakovskii, G. G. Skvortsova, K. V. Zapunnaya, and É. I. Kositsina, Zh. Prikl. Khim.,35, 916 (1962).

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Authors and Affiliations

  1. Irkutsk Institute of Organic Chemistry, Siberian Division of the Academy of Sciences, USSR

    M. F. Shostakovskii, G. G. Skvortsova, E. S. Domnina & N. P. Glazkova

Authors
  1. M. F. Shostakovskii
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  2. G. G. Skvortsova
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  3. E. S. Domnina
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  4. N. P. Glazkova
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 529–531, March, 1965

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Shostakovskii, M.F., Skvortsova, G.G., Domnina, E.S. et al. Peculiarities of the chlorination of vinylindole in halogenation reactions. Russ Chem Bull 14, 504–505 (1965). https://doi.org/10.1007/BF00846613

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  • DOI: https://doi.org/10.1007/BF00846613

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