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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 990453생성일: 2026년 10월 25일

Water → 3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl](3,3,3-trifluoro-2-hydroxypropyl)amino]phenol

https://huagongshe.com/reaction/990453

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-(Trifluoromethyl)oxiraneHCID 520769—
반응물Ytterbium triflateHCID 2733225—
반응물3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]amino]phenolHCID 10958016—
용매AcetonitrileHCID 6342—
생성물3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl](3,3,3-trifluoro-2-hydroxypropyl)amino]phenolHCID 1092806989%

반응 단계

A solution of 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]phenol (11.0 g, 34.9 mmol), 3,3,3-trifluoro-1,2-epoxypropane (4.5 mL, 52.4 mmol) and ytterbium trifluoromethanesulfonate (2.2 g, 10 mol %) in 20 mL of acetonitrile was heated at 50° C. in a sealed glass tube for 16 h. The reaction mixture was cooled, water was added, and the reaction mixture was extracted with ether. The ether layer was washed with saturated aqueous sodium bicarbonate and brine and dried over MgSO4. The dried organic layer was evaporated to give 8.07 g (89%) of the desired 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl](3,3,3-trifluoro-2hydroxypropyl)amino]phenol product as a yellow oil. HRMS calcd. for C18H17F7NO3: 428.1097 [M+H]+, found: 428.1104. 1H NMR (CDCl3) δ 3.58 (dd, 1H), 3.88 (dd, 1H), 4.39 (m, 1H), 4.68 (s, 2H), 5.91 (tt, 1H), 6.25-6.37 (m, 3H), 7.07-7.14 (m, 4H), 7.35 (t, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06458849B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-220ac85b82ec409ab180dff598332e1a
출처 메모uspto-grants-2002_10