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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491466Generated: October 31, 2026

Methyl iodide → 3-Fluoro-4-nitroanisole

https://huagongshe.com/reaction/491466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventAcetoneHCID 180—
Product3-Fluoro-4-nitroanisoleHCID 56565498%

Reaction Steps

To a solution of 3-fluoro-4-nitro-phenol (25.3 g, 0.16 mol) in acetone (160 ml), potassium carbonate (41.7 g, 0.30 mol) and methyl iodide (20.0 ml, 0.32 mol) are added at ambient temperature. The reaction mixture is stirred at 40 C.° for 3 h. After cooling down to room temperature, dichloromethane is added to the reaction mixture, which is filtrated and evaporated. Dichloromethane is added to the residue and the organic phase is washed with H2O and brine, dried over sodium sulfate and evaporated down to give 2-fluoro-4-methoxy-1-nitro-benzene in 98% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531546B2
Source datasetuspto-grants-2009_05
ORD IDord-31d427b164da4674b0c9b430f5361271
Source noteuspto-grants-2009_05