Methyl fluorosulfate → 2-Methyl-2-trifluoromethylperfluoropentane

HRID 1731390

Reaktionsgleichung

Reaktionsgleichung von HRID 1731390
S(F)(OC)(=O)=O.[F:7][C:8]([F:25])([F:24])[C-:9]([C:20]([F:23])([F:22])[F:21])[C:10]([F:19])([F:18])[C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13].[CH3:26]N([S+](N(C)C)N(C)C)C.FC(F)(F)C(C(F)(F)F)=C(F)C(F)(F)C(F)(F)F>C(#N)C1C=CC=CC=1>[F:18][C:10]([F:19])([C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[C:9]([C:20]([F:21])([F:22])[F:23])([C:8]([F:24])([F:25])[F:7])[CH3:26]

Komponenten

5

Versuchsvorschrift

Methyl fluorosulfate (7.6 g, 0.0665 mol) was added dropwise at 0° to a stirred solution of tris(dimethylamino)sulfonium 1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethyl)-2-pentanide, prepared by dissolving 20.2 g (0.073 mol) of tris(dimethylamino)sulfonium difluorotrimethylsilicate and 20.0 g (0.0665 mol) of 1,1,1,3,4,4,5,5,5-nonafluoro-2-trifluoromethyl-2-pentene in 75 mL of benzonitrile. The reaction mixture was warmed at 25°, and the most volatile portion of the reaction mixture was distilled out under reduced pressure. The distillate was redistilled at atmospheric pressure to give 13.27 g (60%) of 3,3,4,4,5,5,5-heptafluoro-2,2-bis(trifluoromethyl)pentane as a colorless liquid: b.p. 88°-89°; 19F NMR (CCl3F) δ -67.7 ppm (t,t, 6F), -81.1 ppm (t, 3F), -110.5 ppm (m, 2F) and -123.7 ppm (m, 2F); 1H NMR (CCl3F) δ1.72 ppm. Anal. Calcd. for C7H3F13 : C, 25.17; H, 0.91; F, 73.93. Found: C, 24.88; H, 0.87; F, 73.64.

Aufarbeitung

  1. customprepared
  2. temperatureThe reaction mixture was warmed at 25°
  3. distillationthe most volatile portion of the reaction mixture was distilled out under reduced pressure
  4. distillationThe distillate was redistilled at atmospheric pressure

Quellen und Nachweise

ORD-Eintrag
ord-ec321684fe534c988cde313a7fa997f0
Quelldatensatz
uspto-grants-1986_11
Patentnummer
US04621126

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