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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485146Generated: October 27, 2026

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

https://huagongshe.com/reaction/485146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant1,1,3,3,3-Pentafluoro-2-(trifluoromethyl)-1-propeneHCID 61109—
ReactantTris(dimethylamino)sulfonium 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)-2-propanideHCID 20228871—
SolventAcetonitrileHCID 6342—
Product[2,2-Bis(trifluoromethyl)-3,3,3-trifluoropropyl]benzeneHCID 1017186681%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535184
Source datasetuspto-grants-1985_08
ORD IDord-7e9982878cec40cfa307d5aa99eb747e
Source noteuspto-grants-1985_08