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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46381Generated: October 29, 2026

Boron tribromide → 1-(2-Hydroxy-5-(trifluoromethyl)phenyl)ethan-1-one

https://huagongshe.com/reaction/46381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant1-(2-Methoxy-5-trifluoromethylphenyl)ethanoneHCID 9942601—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
Product1-(2-Hydroxy-5-(trifluoromethyl)phenyl)ethan-1-oneHCID 1176959935.2%

Reaction Steps

To a stirred solution of 1-[2-methoxy-5-(trifluoromethyl)phenyl]ethanone (35 g, 0.160 mol) in dry dichloromethane (400 mL) at 0° C. was added solid tetrabutylammonium iodide (2.96 g, 0.008 mol) followed by boron tribromide (33.96 mL, 0.353 mol) dropwise. After addition, the reaction mixture was stirred at room temperature for 90 minutes. The reaction mixture was cooled to 0° C. and quenched with ice. The mixture was extracted with diethyl ether (1000 mL). The organic layer was washed with water (2000 mL) and then saturated aqueous sodium chloride (1000 mL). After concentration of the organic layer at room temperature in vacuo, the crude product was purified by column chromatography (100-200 silica gel, 2% v/v diethyl ether in hexane) to give 11.5 g (35%) of the title compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541588B2
Source datasetuspto-grants-2013_09
ORD IDord-70b6a9696d13437a87ea73275552b049
Source noteuspto-grants-2013_09