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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227360Generated: October 27, 2026

Methyl iodide → 4-Bromo-2,6-difluoroanisole

https://huagongshe.com/reaction/227360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2,6-difluorophenolHCID 2736292—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2,6-difluoroanisoleHCID 277328767%

Reaction Steps

Methyl iodide (580 TL, 10.06 mmol) and K2CO3 (2.80 g, 20.12 mmol) were added to a solution of 4-bromo-2,6-difluorophenol (1.05 g, 5.03 mmol) in DMF (10 mL) and stirred at rt under Ar for 24 h. Upon completion, ethyl acetate was added and the reaction was washed with 1% HCl (2×20 mL), brine (1×), dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (hexane) to afford 4-bromo-2,6-difluoroanisole (747 mg, 67%) as a white solid. See, for example, Chambers, R. D.; et al. J. Fluorine Chem. 2000, 102, 169-174, which is incorporated by reference in its entirety. 1H NMR (CDCl3, 400 MHz) δ 7.06 (m, 2H), 3.97 (q, 3H, J=1.1 Hz). 13C NMR (CDCl3, 100 MHz) δ 155.8, 136.3, 116.2, 113.8, 61.9. LREIMS found for C7H5F2OBr (M+) 223.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560488B2
Source datasetuspto-grants-2009_07
ORD IDord-edb684c62abb4e6d8740ebc8b2f54249
Source noteuspto-grants-2009_07