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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006643Generated: November 2, 2026

Furan → Ethyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate

https://huagongshe.com/reaction/1006643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantEthyl AcrylateHCID 8821—
ReactantSodium ThiosulfateHCID 24477—
Catalystzinc(II)iodideHCID 9883512—
SolventEthyl AcetateHCID 8857—
ProductEthyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 1291472252%

Reaction Conditions

Temperature40 °C

Reaction Steps

Furan (2.04 ml, 28 mmol), ethyl acrylate (2.06 ml, 20 mmol) and zinc iodide (1.92 g, 6 mmol) were placed in a sealed tube and the mixture was heated at 40° C. for 2 days. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (100 ml). 10% Aqueous sodium thiosulfate solution (20 ml) was added, and the mixture was stirred at room temperature for 30 min. The organic layer was partitioned, washed with saturated brine (100 ml), and dried over anhydrous sodium sulfate. The components having a low boiling point, such as the solvent and the like, were distilled away. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/10 (volume ratio)) to give 2-ethoxycarbonyl-7-oxabicyclo[2.2.1]hept-5-ene as a mixture of exo form:endo form=7:3 (1.75 g, 10.4 mmol, yield 52.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790964B1
Source datasetuspto-grants-2004_09
ORD IDord-cecc50ac71d44c0fbf37e54cacd035fd
Source noteuspto-grants-2004_09