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Study of the reactivities of methyl esters of furan-2-carboxylic and thiophene-2-carboxylic acids by the method of competitive nitration

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reactivities of methyl esters of furan-2-carboxylic and thiophene-2-carboxylic acidswere studied by the method of competitive nitration. Methyl furan-2-carboxylate is more active in its reactions with a mixture of nitric acid and acetic anhydride (with sulfuric acid as the catalyst) and with a mixture of nitric and sulfuric acids (with acetic anhydride as the solvent).

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, 226006, Riga

    K. K. Venter, M. A. Trushule, V. P. Litvinov, É. G. Ostapenko & É. É. Liepin'sh

Authors
  1. K. K. Venter
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  2. M. A. Trushule
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  3. V. P. Litvinov
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  4. É. G. Ostapenko
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  5. É. É. Liepin'sh
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 601–604, May, 1978.

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Venter, K.K., Trushule, M.A., Litvinov, V.P. et al. Study of the reactivities of methyl esters of furan-2-carboxylic and thiophene-2-carboxylic acids by the method of competitive nitration. Chem Heterocycl Compd 14, 490–493 (1978). https://doi.org/10.1007/BF00673327

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  • DOI: https://doi.org/10.1007/BF00673327

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