Benzyl Bromide → [2,2-Bis(trifluoromethyl)-3,3,3-trifluoropropyl]benzene

HRID 485146

Reaktionsgleichung

Reaktionsgleichung von HRID 485146
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:9][C:10]([F:21])([F:20])[C-:11]([C:16]([F:19])([F:18])[F:17])[C:12]([F:15])([F:14])[F:13].CN([S+](N(C)C)N(C)C)C.FC(F)=C(C(F)(F)F)C(F)(F)F>C(#N)C>[F:9][C:10]([F:20])([F:21])[C:11]([C:12]([F:13])([F:14])[F:15])([C:16]([F:19])([F:18])[F:17])[CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

5

Versuchsvorschrift

Benzyl bromide, 18.8 g (0.11 mol), was added dropwise at 10° to a solution of tris(dimethylamino)sulfonium 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)-2-propanide, prepared by dissolving 24.4 g (0.122 mol) of octafluoroisobutylene and 33.6 g (0.122 mol) of tris(dimethylamino)sulfonium difluorotrimethylsilicate in 75 mL of acetonitrile. The reaction mixture was warmed to 25°, stirred overnight, and then poured into ice water. The aqueous mixture was extracted with ether, and the ether extracts were washed three times with water, dried (MgSO4), and distilled to give 27.35 g (81%) of 3,3,3-trifluoro-2,2-bis(trifluoromethyl)propylbenzene as a colorless liquid, b.p. 53°-54° (12 mm), that solidified on cooling to a white solid: m.p. 32°-33°; 1H NMR (CDCl3) δ 3.39 ppm (s, 2H), 7.28 ppm (s, 5H); 19F NMR (CDCl3) δ -62.3 ppm (s). Anal. Calcd. for C11H7F9 : C, 42.59; H, 2.28; F, 55.13. Found: C, 42.45; H, 2.23; F, 55.00.

Aufarbeitung

  1. customprepared
  2. temperatureThe reaction mixture was warmed to 25°
  3. extractionThe aqueous mixture was extracted with ether
  4. washthe ether extracts were washed three times with water
  5. dry with materialdried (MgSO4)
  6. distillationdistilled

Quellen und Nachweise

ORD-Eintrag
ord-7e9982878cec40cfa307d5aa99eb747e
Quelldatensatz
uspto-grants-1985_08
Patentnummer
US04535184

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