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Functional derivatives of thiophene

V. Synthesis of nitro derivatives of 3-ethoxycarbonyl-4-hydroxy-2-methyl- and 4-chloro-3-ethoxycarbonyl-2-methylthiophenes

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The nitration of 3-ethoxycarbonyl-4-hydroxy-2-methyl- and 4-chloro-3-ethoxycarbonyl-2-methylthiophenes has given the corresponding 5-nitro derivatives of thiophene. The 4-chloro-3-ethoxycarbonyl-2-methylthiophene was synthesized by the decarboxylation of 3-chloro-4-ethoxycarbonyl-5-methylthiophene-2-carboxylic acid, which is formed by the oxidation of 3-chloro-4-ethoxycarbonyl-5-methylthiophene-2-carbaldehyde.

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Literature cited

  1. V. I. Shvedov, O. B. Romanova, V. K. Vasil'eva, V. P. Pakhomov, and A. N. Grinev, Khim. Geterotsikl. Soedin., 741 (1973).

  2. H. Fiesselmann and M. Schorr, German Patent No, 1,137,445; Chem. Abstr., 58, 3398 (1963).

  3. V. I. Shvedov, V. K. Vasil'eva, and A. N. Grinev, Khim. Geterotsikl. Soedin., 427 (1972).

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For Communication IV, see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1024–1025, August, 1973.

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Shvedov, V.I., Vasil'eva, V.K., Romanova, O.B. et al. Functional derivatives of thiophene. Chem Heterocycl Compd 9, 951–952 (1973). https://doi.org/10.1007/BF00471703

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  • DOI: https://doi.org/10.1007/BF00471703

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