Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474678Generated: November 2, 2026

Hydrogen Peroxide → 2-(4-{[3-Chloro-5-(trifluoromethyl)phenyl]oxy}phenyl)ethanol

https://huagongshe.com/reaction/474678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant1-Chloro-3-[(4-ethenylphenyl)oxy]-5-(trifluoromethyl)benzeneHCID 67776939—
SolventTetrahydrofuranHCID 8028—
Product2-(4-{[3-Chloro-5-(trifluoromethyl)phenyl]oxy}phenyl)ethanolHCID 67772774100.3%

Reaction Steps

To the solution of 1-chloro-3-[(4-ethenylphenyl)oxy]-5-(trifluoromethyl)benzene (2.63 g, 8.81 mmol) in dry THF (25 mL), was added 9-BBN (30 mL, 15.00 mmol) at 0° C. The mixture was stirred at room temperature overnight, and quenched with water (2 mL), followed by aq. NaOH (11 mL, 33.0 mmol), and 30% H2O2 (10 mL). The reaction mixture was heated at 50° C. for 3 h. Then THF was removed under reduced pressure, and the residue was diluted with EA. The organic layer was washed with water and brine, dried over anhydrous Na2SO4, concentrated and purified by flash chromatography to afford the title compound (2.8 g, 8.84 mmol, 100% yield) as a colorless oil. LCMS: rt=3.70 min, [M+H+]=299

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-a3d367369951489e80577d4809f70214
Source noteuspto-grants-2014_01