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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238839Generated: October 29, 2026

Iodoethane → Ethyl 3-bromofuran-2-carboxylate

https://huagongshe.com/reaction/2238839

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 numberUS07718808B2
Source datasetuspto-grants-2010_05
ORD IDord-b10647b73ab34b30a881418443d29dbb
Source noteuspto-grants-2010_05