Synthesis of fluorine-containing alkyl 2-cyano-3-oxocarboxylates. Reactions with nucleophiles |
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Authors: | O. G. Kuzueva Ya. V. Burgart V. I. Saloutin O. N. Chupakhin |
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Affiliation: | (1) Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 20 ul. S. Kovalevskoi, 620219 Ekaterinburg, Russian Federation |
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Abstract: | Fluorine-containing alkyl 2-cyano-3-oxocarboxylates were synthesized for the first time by the reaction of ethyl cyanoacetate with fluorine-substituted carboxylic acid halides or alkyl carboxylates. The reactions with hydrazine hydrate, phenylhydrazine, ando-phenylenediamine give hydrazinium (ammonium) enolates or products of acid decomposition. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1961–1965, October, 1999. |
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Keywords: | alkyl perfluoro-2-cyano-3-oxocarboxylates acylation condensation hydrazine hydrate phenylhydrazine o-phenylenediamine salt formation acid decomposition |
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