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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29389Generated: October 30, 2026

Methyl iodide → 5,7-Dichloro-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/29389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5,7-Dichloro-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 68712223—
SolventDimethylformamideHCID 6228—
Product5,7-Dichloro-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 6871245499.3%

Reaction Steps

To 120 mg of 5,7-dichloro-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester was added 1 mL of iodomethane, 200 mg of K2CO3 and 4 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 solution was washed with brine. Removal of the solvent in vacuo gave 125 mg (99% yield) of 5,7-dichloro-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-3ef1fbba0152493389dc72a283a63524
Source noteuspto-grants-2008_09