Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347865Generated: October 25, 2026

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

https://huagongshe.com/reaction/347865

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 numberUS07176216B2
Source datasetuspto-grants-2007_02
ORD IDord-010d34d98dd24f95b563cc8a7cdee595
Source noteuspto-grants-2007_02