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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506144Generated: October 26, 2026

Water → 2-[4-(Trifluoromethyl)phenyl]oxirane

https://huagongshe.com/reaction/1506144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantTrimethylsulfonium iodideHCID 75127—
Reactant1-Ethenyl-4-(trifluoromethyl)benzeneHCID 2782798—
SolventDimethyl SulfoxideHCID 679—
Product2-[4-(Trifluoromethyl)phenyl]oxiraneHCID 999001681%

Reaction Steps

Trimethylsulfonium iodide (4.08 g, 20.0 mmol) in dimethyl sulfoxide (15 mL) was stirred with sodium hydride (55 wt % dispersion in mineral oil, 873 mg, 20.0 mmol) at room temperature for 1 hour and then with 4-(trifluoromethyl)styrene (2.96 g, 17.0 mmol) in dimethyl sulfoxide (10 mL) at room temperature for 2 hours. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1 (v/v)) to give the title compound as a colorless oil (2.59 g, yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-f886d7f436004bc58563b288f1ce0f26
Source noteuspto-grants-2015_12