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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697554Generated: November 4, 2026

Water → 4-Fluoro-2-trifluoromethylbenzenethiol

https://huagongshe.com/reaction/1697554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Fluoro-2-(trifluoromethyl)benzenesulfonyl ChlorideHCID 2737548—
Solvent1,4-DioxaneHCID 31275—
Product4-Fluoro-2-trifluoromethylbenzenethiolHCID 5099800285%

Reaction Conditions

Temperature25 °C

Reaction Steps

4-Fluoro-2-(trifluoromethyl)benzenesulphonyl chloride (2.0 g) was dissolved in dioxane (12 mL) under a N2-atmosphere at ambient temperature. Water (3.0 mL) and tris-(2-carboxylethyl)phosphine hydrochloride (8.73 g) was added afterwards. The reaction mixture is stirred under reflux for 6 h. The reaction mixture is cooled to 25° C. and dissolved with water (30 mL). The product is extracted with CH2Cl2 (100 mL) several times. The combined organic layers are washed with water and dried over Na2SO4. The organic layer is filtrated and evaporated to dryness to yield 1.27 g (85%) of a colorless liquid which is used without further purification. MS (ESI): m/z=194.9 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163793B2
Source datasetuspto-grants-2012_04
ORD IDord-70ace7d7a7c14a90af1d1ee56e3e8411
Source noteuspto-grants-2012_04