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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968668Generated: October 29, 2026

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

https://huagongshe.com/reaction/968668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Benzyloxy-2-fluoro-1-nitrobenzeneHCID 22180704—

Reaction Steps

K2CO3 (8.97 g) and benzylbromide (4.25 mL) were added to a solution of 3-fluoro-4-nitrophenol (5.10 g) in anhydrous DMF (30 mL) at room temperature, and the mixture was stirred overnight. The mixture was diluted with EtOAc and washed with H2O and brine. The organic layer was dried over magnesium sulfate and concentrated. The residual solid was crystallized from EtOAc/hexane to yield 7.31 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304072B2
Source datasetuspto-grants-2007_12
ORD IDord-4cfd45ca7fa6403b9fb60df1ac2da1b8
Source noteuspto-grants-2007_12