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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094808Generated: November 2, 2026

Methyl iodide → 2-Bromo-1-chloro-4-methoxymethyl-benzene

https://huagongshe.com/reaction/1094808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
Reactant(3-Bromo-4-chlorophenyl)methanolHCID 50998689—
Solvent2-MethyltetrahydrofuranHCID 7301—
SolventSodium chloride; waterHCID 57417360—
Product2-Bromo-1-chloro-4-methoxymethyl-benzeneHCID 5758234594%

Reaction Steps

To a stirred solution of 4-chloro-3-bromophenyl-methanol (cited in Amgen patent WO03099776) (900 mg, 4.06 mmol) in 2-methyl-tetrahydrofuran (15 ml) was added potassium hydroxide (912 mg, 16.3 mmol) and the resulting suspension was stirred at room temperature for 30 minutes. Iodomethane (1.01 ml, 4.00 mmol) was then added and the reaction was stirred for 16 hours at room temperature. LCMS indicated incomplete reaction. Potassium hydroxide (912 mg, 16.3 mmol) was added and the resulting mixture stirred for 5 minutes before adding further iodomethane (4.04 ml, 16 mmol) and stirring was continued for 3 hours at room temperature. Ethyl acetate (60 ml) and saturated brine solution (30 ml) were added and the layers were separated. The organic extract was further washed with saturated brine solution (2×30 ml) then dried over anhydrous MgSO4 (s), filtered and evaporated in vacuo to afford the crude title compound as a yellow oil (901 mg, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134007B2
Source datasetuspto-grants-2012_03
ORD IDord-267179f55ba24baf8b8fa5d39c8a28d4
Source noteuspto-grants-2012_03