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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740298Generated: October 27, 2026

Ethyl chloroacetate → Ethyl 4-bromobenzofuran-2-carboxylate

https://huagongshe.com/reaction/1740298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-6-hydroxybenzaldehydeHCID 11954768—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-bromobenzofuran-2-carboxylateHCID 2183810570%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 6-bromo-2-hydroxybenzaldehyde (4.48 g), ethyl chloroacetate (3.55 g) and powdered potassium carbonate (6.16 g) in N,N-dimethylformamide (56 ml) was stirred at 120° C. for one hour. Insoluble materials were filtered off and the solvent was removed under reduced pressure. Ethyl acetate and water were added to the residue, and the mixture was acidified by hydrochloric acid solution. The layers were separated and the organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with a mixture of hexane and toluene (1:1) to afford 4-bromo-2-ethoxycarbonylbenzofuran (4.20 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968985
Source datasetuspto-grants-1999_10
ORD IDord-98fd762db4624387b28eb07581b62cdc
Source noteuspto-grants-1999_10