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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337546Generated: October 25, 2026

Iodoethane → Ethyl 3-bromofuran-2-carboxylate

https://huagongshe.com/reaction/337546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantCesium carbonateHCID 10796—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromofuran-2-carboxylic acidHCID 605479—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-bromofuran-2-carboxylateHCID 2245614954.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Bromofuran-2-carboxylic acid (1.86 g, 9.75 mmol), ethyl iodide (3.1 mL, 38.8 mol) and cesium carbonate (4.80 g, 14.7 mmol) were suspended in acetonitrile (50 mL), followed by stirring at 80° C. for 3 hours. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=9:1) to afford ethyl 3-bromofuran-2-carboxylate (1.16 g, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-a3b9f2d876214edcbe0ca512f91496f6
Source noteuspto-grants-2014_11