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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603889Generated: October 30, 2026

Ethanol → Ethyl (5-bromobenzofuran)-2-carboxylate

https://huagongshe.com/reaction/1603889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant5-Bromo-2-benzofurancarboxylic acidHCID 735247—
ProductEthyl (5-bromobenzofuran)-2-carboxylateHCID 73518493%

Reaction Steps

A solution of 5-bromo-2-benzofurancarboxylic acid (5.01 g, 20.8 mmol) in absolute ethanol (150 ml) was added with concentrated sulfuric acid (15 ml) and the mixture was refluxed under stirring for 2 h. After this time, the volatiles were evaporated off under reduced pressure and the resulting residue was neutralized with a sodium bicarbonate saturated solution and extracted with ethyl ether (4×100 ml). The mixture was dried and the solvent was evaporated off under reduced pressure, to obtain 5.19 g of the title compound as a white solid with melting point 58-60° C. (93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990142
Source datasetuspto-grants-1999_11
ORD IDord-bb9ab76924f3425d8d8322bc3fee41ba
Source noteuspto-grants-1999_11