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Rearrangement of 2,3,5,6-tetrachloro-4-pyridyl β-hydroxyethyl sulfone

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A method for the preparation of 4-mercapto-2,3,5,6-tetrachloropyridine was modified. 2,3,5,6-Tetrachloro-4-pyridyl β-hydroxyethyl sulfone was synthesized and converted to 4-hydroxytetra-chloropyridine by the action of a base. A mechanism for this rearrangement is proposed.

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Literature cited

  1. C. D. S. Tomlin, J. W. Slater, D. Hatley, and C. J. Clayton, British Patent No. 1059990 (1967); Ref. Zh. Khim., 1.0486P (1976).

  2. R. A. Fernandes, H. Heaney, J. M. Jablonski, K. G. Mason, and T. J. Word, J. Chem. Soc., C, 1908 (1969).

    Google Scholar 

  3. L. S. Sologub, S. D. Moshchitskii, Ya. N. Ivashchenko, and Yu. N. Levchuk, Khim. Geterotsikl. Soedin., No. 2, 514 (1962).

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  4. C. K. Ingold, Theoretical Foundations of Organic Chemistry [Russian translation], Moscow (1973), p. 600.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1642–1645, December, 1978.

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Moshchitskii, S.D., Sologub, L.S., Kovalevskaya, T.V. et al. Rearrangement of 2,3,5,6-tetrachloro-4-pyridyl β-hydroxyethyl sulfone. Chem Heterocycl Compd 14, 1334–1337 (1978). https://doi.org/10.1007/BF00487401

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  • DOI: https://doi.org/10.1007/BF00487401

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