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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650183Generated: October 31, 2026

Ethanol → Ethyl 5-bromofuran-2-carboxylate

https://huagongshe.com/reaction/1650183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
ProductEthyl 5-bromofuran-2-carboxylateHCID 345282—

Reaction Steps

To a stirred suspension of 8.43 g (44.14 mmol) of 5-bromo-2-furoic acid in 100 ml absolute ethanol was added 4 ml of thionyl chloride. This mixture was stirred at reflux for 3 hours and at room temperature for 18 hours. The solvent was removed in vacuo, the residual oil treated with 100 ml water and extracted with 3×75 ml ether. The combined ether extracts were washed with saturated NaHCO3 and saturated NaCl solutions and dried (MgSO4). Solvent was removed in vacuo and the residue kugelrohr distilled (60° C.; 0.4 mm) to give the captioned compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923884
Source datasetuspto-grants-1990_05
ORD IDord-6e9379d5bbe64be4b5753b6641dc14eb
Source noteuspto-grants-1990_05