Nitration of perfluoroisobutene

作者: I. L. Knunyants , B. L. Dyatkin , A. V. Fokin , V. A. Komarov

DOI: 10.1007/BF00850330

关键词: TrifluoromethylHydrolysisOrganic chemistryAlcoholNitrogenPerfluoroisobuteneNitrationChemistryNitriteNitrogen dioxide

摘要: 1. The nitration of perfluoroisobutene with nitrogen dioxide at 170–180° gives pentafluoro-3-nitro-2- (trifluoromethyl)-2-propanol nitrous ester (b.p. 109–110°) and a wide fraction 30–100°), which appears to be mixture pentafluoro-2-(trifluoromethyl)-1,2-propanediol dinitrous its transformation products. 2. By the hydrolysis pentafluoro-3-nitro-2-(trifluoromethyl)-2-propanol nitrite alcohol itself was obtained. 3. By 30–100° bistrifluoromethylglycolic [trifluoro-2- (trifluoromethyl)lactic] acid obtained.

参考文章(3)
R. N. Haszeldine, 423. Reactions of fluorocarbon radicals. Part X. Polyfluoroalkyl nitroso- and nitro-compounds Journal of the Chemical Society (Resumed). pp. 2075- 2081 ,(1953) , 10.1039/JR9530002075
D. D. COFFMAN, M. S. RAASCH, G. W. RIGBY, P. L. BARRICK, W. E. HANFORD, ADDITION REACTIONS OF TETRAFLUOROETHYLENE Journal of Organic Chemistry. ,vol. 14, pp. 747- 753 ,(1949) , 10.1021/JO01157A005
EUGENE R. BISSELL, Fluorine-Containing Nitrogen Compounds. III. Some Alkyl Esters of Difluoronitroacetic Acid1 Journal of Organic Chemistry. ,vol. 26, pp. 5100- 5103 ,(1961) , 10.1021/JO01070A075