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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474672Generated: October 26, 2026

Benzyl Bromide → 4-(Benzyloxy)-1-bromo-2-chlorobenzene

https://huagongshe.com/reaction/1474672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3-chlorophenolHCID 7018182—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-1-bromo-2-chlorobenzeneHCID 22319501—

Reaction Steps

4-Bromo-3-chlorophenol (1 g, 4.82 mmol) was dissolved in DMF (10 ml) and K2CO3 (1.332 g, 9.64 mmol) and benzyl bromide (0.630 ml, 5.30 mmol) added. The mixture was stirred under N2 for 1 hr at RT. The mixture was diluted with water (15 mL) and extracted with EtOAc (2×10 mL). The organic fractions were combined, washed with brine (saturated, 1×8 mL), dried over MgSO4, filtered and the volatiles removed in vacuo. The residue was purified by column chromatography on silica gel Biotage 25M, using a gradient eluant of EtOAc/Hexane (0-50%) to afford the title compound. LC/MS (m/z): 297 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018224B2
Source datasetuspto-grants-2015_04
ORD IDord-1d6ff5f57f8744b2af1a5c27066f77da
Source noteuspto-grants-2015_04