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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455901Generated: November 1, 2026

Benzyl Chloride → 1-(Benzyloxy)-3-bromobenzene

https://huagongshe.com/reaction/1455901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromophenolHCID 11563—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-3-bromobenzeneHCID 2756638—

Reaction Steps

A slurry of 3-bromophenol 100 g (580 mmol), benzylchloride 80 g (700 mmol), and K2CO3 168 g (1210 mmol) in 2 L of DMF was stirred for sixteen hour at ambient temperature. The reaction mixture was filtered and evaporated to dryness. The solid was partioned between CHCl3 and water. The organic layer was separated, washed twice with brine, and dried by filtration through anhydrous Na2SO4. The solution was evaporated to dryness. This yielded 142.5 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843940
Source datasetuspto-grants-1998_12
ORD IDord-17ce53964a384ee9b6dc841021b3d8dc
Source noteuspto-grants-1998_12