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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779402Generated: October 30, 2026

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

https://huagongshe.com/reaction/1779402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromophenolHCID 11563—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-3-bromobenzeneHCID 275663889.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under a nitrogen atmosphere, a solution of 50.0 grams (0.29 mole) of 3-bromophenol and 120.0 grams (0.87 mole) of potassium carbonate in 400 mL of N,N-dimethylformamide was stirred, and heated to 80° C. To this was added portionwise, 36.1 mL (0.30 mole) of phenylmethyl bromide during a 20 minute period. Upon completion of addition, the reaction mixture was stirred at 80° C. during a one hour period. After this time, the reaction mixture was allowed to cool to ambient temperature, where it was diluted with 600 mL of water. The mixture was extracted with 600 mL of diethyl ether. The extract was then washed with three 50 mL portions of water, and then it was concentrated under reduced pressure to a residual solid. The solid was recrystallized with 250 mL of methanol, yielding 68.3 grams of 3-(phenylmethoxy)phenyl bromide. The. NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627189
Source datasetuspto-grants-1997_05
ORD IDord-da5e29d180a54664a82e18d39541a7df
Source noteuspto-grants-1997_05