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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801465Generated: October 29, 2026

Benzyl Bromide → 2-(Benzyloxy)-1-fluoro-3-nitrobenzene

https://huagongshe.com/reaction/1801465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-6-nitrophenolHCID 73710—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-1-fluoro-3-nitrobenzeneHCID 68632184102.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-fluoro-6-nitrophenol (25.1 g, 157 mmol) in DMF (430 mL) were added K2CO3 (43.7 g, 313 mmol) and benzyl bromide (21 mL, 172 mmol). The reaction mixture was stirred at 80° C. overnight. After cooling to rt, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure. Water (100 mL) and EA (100 mL) were added and the phases were separated. The aq. layer was extracted once with EA (100 mL) and the combined org. layers were dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was dried under HV to give the title compound as a yellow oil (39.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349828B2
Source datasetuspto-grants-2013_01
ORD IDord-565b562118494767a06fd37e72cbbc81
Source noteuspto-grants-2013_01