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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976317Generated: November 1, 2026

Methyl iodide → 1-Bromo-4-methoxy-2-methylbenzene

https://huagongshe.com/reaction/1976317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-m-cresolHCID 72857—
SolventAcetoneHCID 180—
Product1-Bromo-4-methoxy-2-methylbenzeneHCID 117915—

Reaction Steps

To a solution of 0.8 g (4.4 mmol) of 4-bromo-3-methylphenol in 20 mL of acetone was added 1.5 g (10.9 mmol) of potassium carbonate. A yellow slurry was obtained to which was added 0.55 mL (1.25 g, 8.8 mmol) of methyl iodide. The resultant reaction mixture was stirred at ambient temperature for 12.25 hours, filtered and extracted between ethyl ether and water. The layers were separated and the organic phase was washed with sat. Na2SO3 (aq.) solution, dried over MgSO4, filtered and then concentrated in vacuo to a yellow oil. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225494B1
Source datasetuspto-grants-2001_05
ORD IDord-ab3c4f1fb2254098958d5089c785a58e
Source noteuspto-grants-2001_05