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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48075생성일: 2026년 10월 23일

2-(Trifluoromethyl)oxirane → 3-[(2,5-Difluorophenyl)[[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol

https://huagongshe.com/ko/reaction/48075

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참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)oxiraneHCID 520769—
반응물N-(2,5-difluorophenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-methyl]amineHCID 11002165—
촉매Ytterbium triflateHCID 2733225—
용매AcetonitrileHCID 6342—
생성물3-[(2,5-Difluorophenyl)[[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanolHCID 2350607184%

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온도50 °C

반응 단계

Ex-661B) The N-(2,5-difluorophenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]-amine (2.22 g, 6.67 mmol) product from EX-661A and 1,1,1-trifluoro-2,3-epoxypropane (1.12 g, 10 mmol) were dissolved in 1.5 mL of acetonitrile. Ytterbium (III) trifluoromethanesulfonate (0.21 g, 0.33 mmol) was added, and the stirred solution was warmed to 50° C. for 2 h under an atmosphere of nitrogen, at which time HPLC analysis indicated that no secondary amine starting material remained. The reaction was quenched with water and extracted with ether. The ether layer was washed with water and brine, then dried over anhydrous MgSO4. The crude product was purified by flash column chromatography on silica gel eluting with ethyl acetate in hexane (1:10) to give 2.49 g (84%) of the desired 3-[(2,5-difluorophenyl)[[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol product as a yellow oil, 99% pure by HPLC analysis. HRMS calcd. for C18H14F9NO2: 448.0959 [M+H]+, found: 448.0940.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699898B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-2ad2d8b451be40fd911073ab83b12020
출처 메모uspto-grants-2004_03