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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042091Generated: October 29, 2026

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

https://huagongshe.com/reaction/1042091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-4-fluoro-1-nitrobenzeneHCID 1109690898%

Reaction Steps

To a mixture of 5-fluoro-2-nitrophenol (50.0 g), potassium carbonate (44.0 g) and N,N-dimethylformamide (150 mL) was added under ice-cooling benzyl bromide (59.9 g), and the mixture was stirred at room temperature for 15 hr. The reaction solution was concentrated under reduced pressure, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained solid was washed with hexane to give the title compound (77.1 g, yield 98%) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-3e3107e0ff74425ea8af7f803966451e
Source noteuspto-grants-2013_10