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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593072Generated: October 30, 2026

Benzyl Bromide → 2-(Benzyloxy)-4-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/1593072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantCesium carbonateHCID 10796—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-(Benzyloxy)-4-fluoro-1-nitrobenzeneHCID 11096908—

Reaction Steps

A mixture of 5-fluoro-2-nitro-phenol (464 mg, 2.95 mmol), benzyl bromide (0.37 ml, 3.10 mmol) and cesium carbonate (1.055 g, 3.24 mmol) in MeCN (10 mL) was stirred room temperature under argon for 48 hours. The reaction mixture was diluted with ethyl acetate and washed with brine. The organic layers were combined and concentrated in vacuo to give a crude residue, which was purified by column chromatography (silica 5-25% EtOAc/hexane) to give 2-benzyloxy-4-fluoro-1-nitro-benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294635B2
Source datasetuspto-grants-2007_11
ORD IDord-0f00944ef9194a7694c17afbe89eb51b
Source noteuspto-grants-2007_11