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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667302Generated: October 31, 2026

Methyl iodide → 2-Bromo-5-methoxy-1,3-dimethylbenzene

https://huagongshe.com/reaction/1667302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3,5-dimethylphenolHCID 81970—
SolventAcetoneHCID 180—
Product2-Bromo-5-methoxy-1,3-dimethylbenzeneHCID 23599285.8%

Reaction Steps

After 10.4 g of potassium carbonate and 6.80 ml of methyl iodide were added to a solution of 10.0 g of 4-bromo-3,5-dimethylphenol in 100 ml of acetone, the mixture was heated under reflux for 15 hours. The reaction mixture was concentrated under reduced pressure and saturated aqueous ammonium chloride was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated and the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 9.18 g of 4-bromo-3,5-dimethylanisole as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044206B2
Source datasetuspto-grants-2011_10
ORD IDord-3cda5ca34ab4484fb01948da5fa665c5
Source noteuspto-grants-2011_10