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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846012Generated: November 1, 2026

Methyl iodide → 2-Bromo-5-fluoroanisole

https://huagongshe.com/reaction/1846012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-fluorophenolHCID 2724600—
SolventDimethylformamideHCID 6228—
Product2-Bromo-5-fluoroanisoleHCID 701804393%

Reaction Steps

To a pre-cooled suspension of 2-bromo-5-fluorophenol (5 g, 26.18 mmol) and potassium carbonate (10.84 g, 78.54 mmol) in DMF (15 mL) at 0-5° C., was added methyl iodide (4.75 mL, 39.27 mmol) and the resulting reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was partitioned between water (20 mL) and EtOAc (50 mL). The organic layer was separated and the aqueous layer was further extracted with EtOAc (3×50 mL). The organic layers were combined, washed with saturated brine solution (20 mL) and dried over Na2SO4, filtered and concentrated in vacuo to afford 1-bromo-4-fluoro-2-methoxybenzene as a colourless liquid in 93% yield, 5.00 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952008B2
Source datasetuspto-grants-2015_02
ORD IDord-97f07a49841b4a15b30b4fbd6be17c07
Source noteuspto-grants-2015_02