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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253399Generated: October 31, 2026

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

https://huagongshe.com/reaction/2253399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium MethoxideHCID 10942334—
Reactant(4-Bromo-3,5-dimethoxyphenyl)methanolHCID 11149289—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 2308094099.5%

Reaction Steps

Mesyl chloride (34.5 mL, 446 mmol) was added to a solution of (4-bromo-3,5-dimethoxyphenyl)methanol (100 g, 405 mmol) and triethylamine (67.5 mL, 484 mmol) in 1,2-dimethoxyethane (1000 mL) while cooling with ice, and the reaction mixture was stirred for 30 minutes. After adding a 28% sodium methoxide in methanol (350 mL, 1.72 mol) to the reaction mixture, it was further stirred for 3 hours at room temperature. Upon completion of the reaction, toluene (1000 mL) and water (1000 mL) were added to the reaction mixture, the aqueous layer was removed, and the organic extract was washed with water (1000 mL), 1N hydrochloric acid (500 mL) and water (500 mL) in that order and concentrated under reduced pressure to afford 105 g of the title compound as a colorless oil (99.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323569B2
Source datasetuspto-grants-2008_01
ORD IDord-581fa21972a34291bf12ca933a48f668
Source noteuspto-grants-2008_01