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HRID 50466Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/50466

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-(Trifluoromethyl)oxiraneHCID 520769—
EduktYtterbium triflateHCID 2733225—
Edukt3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]amino]phenolHCID 10958016—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl](3,3,3-trifluoro-2-hydroxypropyl)amino]phenolHCID 1092806989%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710089B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-85c05d1f5d23403c9f3214da01ee59db
Quellennotizuspto-grants-2004_03