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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990519Generated: October 30, 2026

2-(Trifluoromethyl)oxirane → 3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]-(3,3,3-trifluoro-2-hydroxypropyl)amino]benzonitrile

https://huagongshe.com/reaction/990519

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)oxiraneHCID 520769—
ReactantYtterbium triflateHCID 2733225—
Reactant3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]amino]benzonitrileHCID 23506027—
SolventAcetonitrileHCID 6342—
Product3-[[[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]methyl]-(3,3,3-trifluoro-2-hydroxypropyl)amino]benzonitrileHCID 2350604276%

Reaction Conditions

Temperature50 °C

Reaction Steps

The benzonitrile (1.58 g, 4.88 mmol) from EX-576A and 1,1,1-trifluoro-2,3-epoxy-propane (546 mL, 6.34 mmol) were dissolved in 4 mL of acetonitrile. Ytterbium (III) trifluoromethanesulfonate (304 mg, 0.49 mmol) was added, and the stirred solution was warmed to 50° C. overnight. The reaction was quenched with water and extracted with ether. The ether layer was washed with brine, dried over MgSO4 and evaporated. The crude product was purified by MPLC on silica gel eluting with dichloromethane to give 1.61 g (76%) of the desired 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]-(3,3,3-trifluoro-2-hydroxypropyl)amino]benzonitrile product as a clear oil, greater than 98% by reverse phase HPLC. HRMS calcd. for C19H15F7N2O2: 437.1100 [M+H]+, found: 437.1097. 1H NMR (CDCl3) δ3.60-3.69 (m, 1H), 3.86 (d, 1H), 4.32 (bs, 1H), 4.69 (q, 2H), 5.86 (dt, 1H), 6.85-6.95 (m, 2H), 6.97-7.01 (m, 2H), 7.04-7.12 (m, 2H), 7.23-7.37 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458852B1
Source datasetuspto-grants-2002_10
ORD IDord-59dd92fb2a4741208495a458c29e1e9d
Source noteuspto-grants-2002_10