STUDIES ON ISOXAZOLE AND PYRAZOLE FORMATION BY THE REACTION OF TRIFLUOROMETHYL-SUBSTITUTED ANILINES WITH OXIME AND HYDRAZONE DIANIONS

Citation
L. Strekowski et Sy. Lin, STUDIES ON ISOXAZOLE AND PYRAZOLE FORMATION BY THE REACTION OF TRIFLUOROMETHYL-SUBSTITUTED ANILINES WITH OXIME AND HYDRAZONE DIANIONS, Journal of heterocyclic chemistry, 34(5), 1997, pp. 1625-1627
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0022152X
Volume
34
Issue
5
Year of publication
1997
Pages
1625 - 1627
Database
ISI
SICI code
0022-152X(1997)34:5<1625:SOIAPF>2.0.ZU;2-V
Abstract
5-(2-Aminophenyl)isoxazoles are obtained in good yields by the reactio n of 2-(trifluoromethyl) aniline with dilithio derivatives of oximes o f acetone, 3-pentanone, propiophenone, and cyclohexanone. An analogous synthesis of a substituted isoxazole from 4-(trifluoromethyl)aniline and 3-pentanone oxime and the synthesis of a substituted pyrazole from 2-(trifluoromethyl)aniline and 3-pentanone hydrazone are less efficie nt.