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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883469Generated: October 30, 2026

1-Chloro-4-(trifluoromethyl)benzene → HCID 2760769, compound

https://huagongshe.com/reaction/1883469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
ReactantPotassium CarbonateHCID 11430—
ReactantMercapto-ethanolHCID 4713212—
SolventDimethylformamideHCID 6228—
ProductHCID 2760769HCID 276076967.6%

Reaction Steps

4-Chlorobenzotrifluoride (31.36 ml, 235.26 mmol) was dissolved in anhydrous DMF (200 ml), and mercaptoethanol (15.00 ml, 213.87 mmol) and K2CO3 (38.43 g, 278.06 mmol) were added thereto. The mixture was stirred for 30 minutes at room temperature and then refluxed. After 15 hours have passed, the reaction mixture was cooled to room temperature and the reaction was stopped by adding distilled water. The reaction mixture was extracted with diethyl ether, and the organic layer was washed with aqueous NH4Cl solution, dried over anhydrous MgSO4, and concentrated. The reaction solution thus concentrated was purified by silica gel column chromatography (EA/n-hexane=1/3, v/v) to give 2-(4-trifluoromethyl-phenylsulfanyl)-ethanol (32.11 g, 67.56%) of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759511B2
Source datasetuspto-grants-2004_07
ORD IDord-51206e095d7f4ef1bcfdf8aa61a46064
Source noteuspto-grants-2004_07