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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 990492생성일: 2026년 10월 26일

2-(Trifluoromethyl)oxirane → 3-[[3-(4-Fluorophenoxy)phenyl][[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol

https://huagongshe.com/reaction/990492

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참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)oxiraneHCID 520769—
반응물N-[3-(4fluorophenoxy)phenyl][[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amineHCID 23505995—
촉매Ytterbium triflateHCID 2733225—
용매AcetonitrileHCID 6342—
생성물3-[[3-(4-Fluorophenoxy)phenyl][[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanolHCID 1022980881%

반응 조건

온도40 °C

반응 단계

The N-[3-(4fluorophenoxy)phenyl][[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amine (612 mg, 1.5 mmol) product from EX-634C and 1,1,1-trifluoro-2,3-epoxypropane (268 mg, 2.4 mmol) were dissolved in 1.0 mL of acetonitrile. Ytterbium (III) trifluoromethanesulfonate (43 mg, 0.07 mmol) was added, and the stirred solution was warmed to 40° C. for 2.5 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 brine and water, then dried over anhydrous MgSO4. The ether was removed in vacuo, and the crude product was purified by flash column chromatography on silica gel eluting with ethyl acetate in hexane (1:11) to give 633 mg (81%) of the desired 3-[[3-(4-fluorophenoxy)phenyl][[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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06458849B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-4be35cab2d9e4102b44674619c2db543
출처 메모uspto-grants-2002_10