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HRID 50466作成日:2026年10月25日

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

https://huagongshe.com/reaction/50466

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-(Trifluoromethyl)oxiraneHCID 520769—
反応物Ytterbium triflateHCID 2733225—
反応物3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]amino]phenolHCID 10958016—
溶媒AcetonitrileHCID 6342—
生成物3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl](3,3,3-trifluoro-2-hydroxypropyl)amino]phenolHCID 1092806989%

反応手順

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-2-hydroxypropyl)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), 735 (t, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710089B2
出典データセットuspto-grants-2004_03
ORD IDord-85c05d1f5d23403c9f3214da01ee59db
出典メモuspto-grants-2004_03