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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850718Generated: November 3, 2026

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

https://huagongshe.com/reaction/1850718

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 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 numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-045cb08c5c874fb589dbe5ee1c14f47a
Source noteuspto-grants-2015_02