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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967875Generated: November 2, 2026

Iodoethane → Ethyl 3-bromofuran-2-carboxylate

https://huagongshe.com/reaction/1967875

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 numberUS08420827B2
Source datasetuspto-grants-2013_04
ORD IDord-2063cc0694ad4bb2a14492062ec71669
Source noteuspto-grants-2013_04