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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705916Generated: October 31, 2026

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

https://huagongshe.com/reaction/705916

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 numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-05a38ac9da4d4f8db1a291d3990889f9
Source noteuspto-grants-2015_11