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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20065Generated: October 25, 2026

Boron tribromide → 3-Bromo-4-fluorobenzyl Bromide

https://huagongshe.com/reaction/20065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—
SolventDichloromethaneHCID 6344—
Product3-Bromo-4-fluorobenzyl BromideHCID 12922710—

Reaction Steps

(3-Bromo-4-fluorophenyl)methanol (0.264 g, 1.29 mmol) was dissolved in DCM (3 mL). The solution was cooled to 0 deg, and tribromoborane (1.0 M in DCM, 0.863 ml, 0.863 mmol) was added. The mixture was stirred at 0 deg for 1 h, then rt for 1 h. The reaction was quenched with water, and the mixture was transferred to a separatory funnel with half-saturated NaHCO3 (15 mL), and the aqueous phase was extracted with DCM (3×20 mL). The organics were combined, washed with half-saturated brine (5 mL), dried over sodium sulfate and concentrated. Purification of the residue through silica gel (40 mL) using 5% EtOAc-hexane afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745484B2
Source datasetuspto-grants-2010_06
ORD IDord-bdee873a287547a4bb709c42021939a4
Source noteuspto-grants-2010_06