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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29399Generated: October 30, 2026

Methyl iodide → 5-Bromo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/29399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 12542970—
SolventDimethylformamideHCID 6228—
Product5-Bromo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 6871597588.2%

Reaction Steps

To 200 mg (0.67 mmol) of 5-bromo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester was added 0.5 mL of iodomethane, 200 mg of K2CO3 and 2 mL of DMF. The mixture was stirred at room temperature overnight. The mixture was washed with brine and extracted with ethyl acetate. The combined ethyl acetate layers were washed with brine. Removal of the solvent in vacuo gave 185 mg (88% yield) of 5-bromo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-c40dd3f64f5d4e6bb18e4e6f9c268dd7
Source noteuspto-grants-2008_09