Study of the reaction of fluoroalkyl ?-ketoesters with methylhydrazine by1H and19F NMR spectroscopy

Autor: Viktor I. Saloutin, M. I. Kodess, A. N. Fomin, B. A. Ershov, S. I. Selivanov, K. I. Pashkevich
Rok vydání: 1988
Předmět:
Zdroj: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:318-321
ISSN: 1573-9171
0568-5230
DOI: 10.1007/bf00957434
Popis: By1H and19F NMR spectroscopy it was shown that reaction of fluoroalkyl β-ketoesters with methylhydrazine in deuteromethanol at −30 to 30‡C involves intermediate formation of the β-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.
Databáze: OpenAIRE