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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248986Generated: November 2, 2026

Water → BENZYL TRIFLUOROMETHYL SULFIDE

https://huagongshe.com/reaction/1248986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantHCID 10236270HCID 10236270—
SolventAcetonitrileHCID 6342—
ProductBENZYL TRIFLUOROMETHYL SULFIDEHCID 378277582%

Reaction Steps

Benzyl bromide, 16.2 g (0.095 mol), was added dropwise at 25° to 0.11 mol of tris(dimethylamino)sulfonium trifluoromethanethiolate (prepared as in Example 11) in 75 mL of acetonitrile. The reaction mixture was stirred one h and then poured into water. The aqueous mixture was extracted with ether, and the ether extracts were washed with water, dried (MgSO4), and distilled to give 15.1 g (82%) of benzyl trifluoromethyl sulfide as a colorless liquid: bp 55° (12 mm); 1H NMR (CDCl3) δ4.08 ppm (s, 2H), 7.33 ppm (s, 5H); 19F NMR (CDCl3) δ-42.5 ppm (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628094
Source datasetuspto-grants-1986_12
ORD IDord-76984f4682874ec0a78204c703a01e7e
Source noteuspto-grants-1986_12