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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188869Generated: November 1, 2026

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

https://huagongshe.com/reaction/1188869

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 benzyl bromide (59.9 g) under ice-cooling, and the mixture was stirred for 15 hr. The reaction mixture was concentrated under reduced pressure, water was added, and the mixture was subjected to extraction 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 numberUS08673942B2
Source datasetuspto-grants-2014_03
ORD IDord-35b7b4408343412aa17ea13e7bc06d5d
Source noteuspto-grants-2014_03