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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515895Generated: October 30, 2026

Benzyl Bromide → 4-(benzyloxy)-N-phenylaniline

https://huagongshe.com/reaction/515895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant4-HydroxydiphenylamineHCID 31208—
SolventAcetonitrileHCID 6342—
Product4-(benzyloxy)-N-phenylanilineHCID 296079—

Reaction Steps

To a solution of 4-hydroxy-N-phenyl-aniline (30 g; 162 mmol) in acetonitrile (400 mL) there are added 58 g of Cs2CO3 (178 mmol) and stirring is carried out for 15 minutes at ambient temperature. Benzyl bromide (22.5 mL; 178 mmol) is then added dropwise and then the reaction mixture is refluxed for 4 hours. After filtering and rinsing with acetonitrile, the filtrate is concentrated and purified by chromatography over silica gel using petroleum ether and ethyl acetate as eluants. The title product is then obtained in the form of a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-e33c16b7ac2b48169432ff3da3fed603
Source noteuspto-grants-2015_08