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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518673Generated: October 30, 2026

Potassium Carbonate → 2-Fluoro-4-(4-methoxybenzyloxy)-1-nitrobenzene

https://huagongshe.com/reaction/518673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Fluoro-4-(4-methoxybenzyloxy)-1-nitrobenzeneHCID 60196087—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 3-fluoro-4-nitrophenol (2.96 g, 18.81 mmol) in DMF (18.81 mL) was added 1-(chloromethyl)-4-methoxybenzene (2.55 mL, 18.81 mmol) and potassium carbonate (5.20 g, 37.6 mmol). The reaction mixture was stirred at 50° C. for 16 hours. The mixture was diluted with EtOAc (100 mL), washed with water, and the aqueous layer was back-extracted with EtOAc (25 mL). The combined organic layers were washed with 1 M aqueous NaOH (20 mL) and then with brine. The organic layer was dried over Na2SO4, filtered and evaporated. The yellow solid was triturated with ether (20 mL), and the solid was collected, rinsing with ether (5 mL). The title compound was obtained as a yellow solid (4.39 g, 84% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-2ce96882ba7f48739399664c791b5c9b
Source noteuspto-grants-2015_08