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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2233441생성일: 2026년 10월 24일

Hydrochloric Acid → 2,2,2-Trifluoro-1-(4-furan-3-yl-phenyl)-ethanol

https://huagongshe.com/ko/reaction/2233441

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물4-(Furan-3-Yl)BenzaldehydeHCID 21526045—
용매TetrahydrofuranHCID 8028—
생성물2,2,2-Trifluoro-1-(4-furan-3-yl-phenyl)-ethanolHCID 6674360483.3%

반응 단계

Tetrabutylammonium fluoride (0.024 ml; 1.0 M solution in tetrahydrofuran) was added to a solution of 4-furan-3-yl-benzaldehyde (410 mg, 2.38 mmol) and trifluoromethyltrimethylsilane (TMSCF3) (423 μl, 2.86 mmol) in 5 ml THF at 0° C. The formed mixture was warmed up to room temperature and stirred at room temperature for 4 hours. The reaction mixture was then treated with 5 ml of 1N HCl and stirred at room temperature overnight. The product was extracted with ethyl acetate (3×50 ml). The organic layer was separated and dried over sodium sulfate. The organic solvent was evaporated to give 480 mg of 2,2,2-trifluoro-1-(4-furan-3-yl-phenyl)-ethanol, yield: 83%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07709493B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-40025981711845388561bed90ec8df1f
출처 메모uspto-grants-2010_05