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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890448Generated: October 31, 2026

Boron trifluoride etherate → 4-Bromo-1-chloro-2-(4-methoxybenzyl)benzene

https://huagongshe.com/reaction/1890448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylsilaneHCID 12052—
ReactantPotassium HydroxideHCID 14797—
Reactant(5-Bromo-2-chloro-phenyl)-(4-ethoxy-phenyl)-methanoneHCID 22328608—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-chloro-2-(4-methoxybenzyl)benzeneHCID 22328594—

Reaction Conditions

Temperature47.5 °C

Reaction Steps

A solution of 86.2 g (5-bromo-2-chloro-phenyl)-(4-methoxy-phenyl)-methanone and 101.5 mL triethylsilane in 75 mL dichloromethane and 150 mL acetonitrile is cooled to 10° C. Then with stirring 50.8 mL of boron trifluoride etherate are added so that the temperature does not exceed 20° C. The solution is stirred for 14 h at ambient temperature, before another 9 mL triethylsilane and 4.4 mL boron trifluoride etherate are added. The solution is stirred for a further 3 h at 45-50° C. and then cooled to ambient temperature. A solution of 28 g potassium hydroxide in 70 mL water is added and the mixture is stirred for 2 h. Then the organic phase is separated and the aqueous phase is extracted three times with diisopropylether. The combined organic phases are washed twice with 2 M potassium hydroxide solution and once with brine and then dried over sodium sulfate. After the solvent has been eliminated the residue is stirred in ethanol, separated off again and dried at 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507450B2
Source datasetuspto-grants-2013_08
ORD IDord-825d2917b9d04961b8765c25eea43827
Source noteuspto-grants-2013_08