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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1635722생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1635722

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Sodium CarbonateHCID 10340—
반응물4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
반응물1-Bromo-3-(cyclopentylthio)benzeneHCID 22170879—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물[3-(4-Trifluoromethylphenyl)phenyl]cyclopentyl sulfideHCID 1780897278%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06509354B1
출처 데이터셋uspto-grants-2003_01
ORD IDord-70412866f4b043599a535c5712ce26f9
출처 메모uspto-grants-2003_01