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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41243Generated: October 25, 2026

Dichloromethane → 2-Bromo-5-(chloromethyl)-1,3-dimethoxybenzene

https://huagongshe.com/reaction/41243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(4-Bromo-3,5-dimethoxyphenyl)methanolHCID 11149289—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventEthylacetate heptaneHCID 21899848—
Product2-Bromo-5-(chloromethyl)-1,3-dimethoxybenzeneHCID 24971972—

Reaction Steps

To a mixture of (4-bromo-3,5-dimethoxyphenyl)methanol (10.0 g, 40.6 mmol) and dichloromethane (100 mL) were added triethylamine (12.4 mL, 89.3 mmol) and methanesulfonyl chloride (3.46 mL, 44.7 mmol) in this order while cooling on ice, and the mixture was stirred at room temperature for 14 hours. To the mixture was added water, and then ethyl acetate was added. After thoroughly shaking the mixture, the organic layer was separated, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=4/1) to obtain the title compound (2.47 g, 9.30 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530504B2
Source datasetuspto-grants-2013_09
ORD IDord-9fdee2737a0e4f69bbfa35d7e843adc0
Source noteuspto-grants-2013_09