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Study of the reaction of fluoroalkyl β-ketoesters with methylhydrazine by1H and19F NMR spectroscopy
Authors:V. I. Saloutin  M. I. Kodess  A. N. Fomin  S. I. Selivanov  B. A. Ershov  K. I. Pashkevich
Affiliation:(1) Institute of Chemistry, Ural Branch, Academy of Sciences of the USSR, USSR
Abstract:Conclusions By1H and19F NMR spectroscopy it was shown that reaction of fluoroalkyl beta-ketoesters with methylhydrazine in deuteromethanol at –30 to 30DaggerC involves intermediate formation of the beta-ketoester salts with methylhydrazine and 3,5-dioxypyrazolidines which successively split off methanol and H2O with formation of 3-oxypyrazolines and pyrazol-5-ones, respectively.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 399–402, February, 1988.
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