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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253402Generated: October 30, 2026

Methyl iodide → 2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzene

https://huagongshe.com/reaction/2253402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant(4-Bromo-3,5-dimethoxyphenyl)methanolHCID 11149289—
SolventDimethylformamideHCID 6228—
Product2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 23080940—

Reaction Steps

Sodium hydride (60% in oil; 24.7 g) was added to a solution of (4-bromo-3,5-dimethoxyphenyl)methanol (118.8 g) in N,N-dimethylformamide (960 mL) while cooling with ice, and after stirring for 10 minutes, iodomethane (41.7 mL) was added dropwise, the temperature was increased to room temperature and stirring was continued for 1 hour. The obtained reaction mixture was poured into ice water (2.5 L), extraction was performed with ethyl acetate, the extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (121.3 g) was obtained as a colorless oil from the n-hexane:ethyl acetate (4:1) fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323569B2
Source datasetuspto-grants-2008_01
ORD IDord-9611bc61c2bf4609a9047e035150afa1
Source noteuspto-grants-2008_01