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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635722Generated: October 25, 2026

Toluene → [3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfide

https://huagongshe.com/reaction/1635722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant1-Bromo-3-(cyclopentylthio)benzeneHCID 22170879—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product[3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfideHCID 1780897278%

Reaction Steps

1.0 g (5.2 mmol) of 4-trifluoromethylphenyl boronic acid, 1.4 g (5.4 mmol) of 3-bromophenyl cyclopentyl sulfide, 1.6 g (15.0 mmol) of sodium carbonate and 0.8 g (0.7 mmol) of tetrakis(triphenylphosphine) palladium were added to a solvent mixture of 50 ml of toluene, 25 ml of ethanol and 25 ml of water and refluxed under heating and stirring for 2 hours. The resulting reaction mixture was poured into ice-cold water and extracted with toluene. The toluene layer was washed with water twice and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 1.3 g of [3-(4-trifluoromethylphenyl)phenyl]cyclopentyl sulfide (yield 78.0%) as a colorless liquid (nD20 1.5732).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509354B1
Source datasetuspto-grants-2003_01
ORD IDord-70412866f4b043599a535c5712ce26f9
Source noteuspto-grants-2003_01