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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V. I. Shvedov, O. B. Romanova, V. K. Vasil'eva, V. P. Pakhomov, and A. N. Grinev, Khim. Geterotsikl. Soedin., 741 (1973).
H. Fiesselmann and M. Schorr, German Patent No, 1,137,445; Chem. Abstr., 58, 3398 (1963).
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