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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8426생성일: 2026년 10월 23일

4-Methylbenzophenone → 4-Methyl-alpha-phenyl-alpha-(trifluoromethyl)benzenemethanol

https://huagongshe.com/ko/reaction/8426

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylbenzophenoneHCID 8652—
반응물Phenyl Trifluoromethyl SulfoneHCID 555605—
반응물HCID 178418922HCID 178418922—
용매DimethylformamideHCID 6228—
생성물4-Methyl-alpha-phenyl-alpha-(trifluoromethyl)benzenemethanolHCID 1196169985%

반응 조건

온도-50 °C

반응 단계

Into a dry Schlenk flask under an argon atmosphere, was added 7 mL DMF solution of phenyl trifluoromethyl sulfone (1a, 420 mg, 2 mmol) and 4-methylbenzophenone (196 mg, 1 mmol) at −50° C., was added 3 mL DMF solution of tBuOK (280 mg, 2.5 mmol). The reaction flask was then sealed and the reaction mixture was then stirred from −50° C. for 1 h, followed by stirring at −50° C. to room temperature overnight. The reaction mixture was quenched with 10 mL of ice water, and extracted with ether (20 ml×3). The combined ether phase was washed with saturated NH4Cl aqueous solution, followed by washing with water. After drying over MgSO4, the ether solvent was removed under vacuum. The crude product was further purified by column chromatography (hexanes/ether=9/1) to give 225 mg of product, 4-methyl-α-phenyl-α-(trifluoromethyl)benzenemethanol as a colorless oily liquid, yield 85%. 1H NMR (CDCl3): δ 2.36 (s, 3H); 2.89 (s, 1H); 7.17–7.51 (m, 9H). 19F NMR (CDCl3): δ −74.4. MS: 266 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087789B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-22e1ed36935945f98fd23107fff48bed
출처 메모uspto-grants-2006_08