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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593070Generated: October 31, 2026

Methyl iodide → 5-Fluoro-2-nitroanisole

https://huagongshe.com/reaction/1593070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantCesium carbonateHCID 10796—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-2-nitroanisoleHCID 2779250—

Reaction Steps

To a solution of 5-fluoro-2-nitro-phenol (369 mg, 2.35 mmol) in 5 mL THF, sodium hydride (96 mg, 2.46 mmol) was added at room temperature, followed by methyl iodide (0.88 ml, 14 mmol). The mixture was stirred at room temperature for 10 hours, and then cesium carbonate (744 mg, 2.35 mmol) was added. The mixture was stirred at room temperature for additional 4 hours, then diluted with ethyl acetate and washed with brine. The organic layers were combined and concentrated in vacuo to give a crude residue, which was purified by column chromatography (silica 5-25% EtOAc/hexane) to give pure 4-fluoro-2-methoxy-1-nitro-benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294635B2
Source datasetuspto-grants-2007_11
ORD IDord-24a5e9f2f62d4277831c88d80521f9a4
Source noteuspto-grants-2007_11