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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1988063생성일: 2026년 10월 25일

Hydrochloric Acid → 2,2,2-Trifluoro-1-(2-furan-3-yl-phenyl)-ethanol

https://huagongshe.com/reaction/1988063

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물2-(Furan-2-yl)benzaldehydeHCID 2772294—
생성물2,2,2-Trifluoro-1-(2-furan-3-yl-phenyl)-ethanolHCID 6674368890%

반응 단계

Tetrabutylammonium fluoride (0.1 ml of 1M in THF) was added to a solution of 2-furan-2-yl-benzaldehyde (123 mg, 0.71 mmol) and trifluoromethyl trimethylsilane (120 mg, 0.86 mmol) in 10 ml THF at 0° C. The mixture was warmed up to room temperature and stirred for 4 hours. The reaction mixture was then treated with 3 ml of 1 M HCl and stirred overnight. The product was extracted with ethyl acetate (3×20 ml). The organic layer was separated and dried over sodium sulfate. The organic solvent was evaporated to give 0.150 g of 2,2,2-trifluoro-1-(2-furan-3-yl-phenyl)-ethanol, which was directly used in next step without purification (yield: 90%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07553840B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-15c1d83a9d934e68a6d8646b770729a6
출처 메모uspto-grants-2009_06