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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947931Generated: November 3, 2026

Methyl iodide → 2-Fluoro-6-nitroanisole

https://huagongshe.com/reaction/1947931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-6-nitrophenolHCID 73710—
SolventDimethylformamideHCID 6228—
Product2-Fluoro-6-nitroanisoleHCID 598606101%

Reaction Steps

A solution of 2-fluoro-6-nitrophenol (10.0 g, 63.6 mmol) in DMF (25.0 mL) was charged with methyl iodide (5.94 mL, 95.5 mmol) and potassium carbonate (13.2 g, 95.5 mmol). The reaction mixture was stirred at rt for 16 h. The reaction was quenched with water (30 mL) and extracted with EtOAc (30 mL). The organic layer was washed with water (25 mL), washed with Brine (25 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to yield a brown oil, 11.0 g (101% yield). 1H NMR (CDCl3, 400 MHz): δ=4.08 (d, J=2.02 Hz, 3H), 7.14 (td, J=8.34, 4.80 Hz, 1H), 7.35 (ddd, J=10.74, 8.34, 1.64 Hz, 1H), 7.58 (dt, J=8.27, 1.55 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-0376f00ada7145cbb2a218ea98e605ce
Source noteuspto-grants-2013_03