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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250753Generated: November 1, 2026

Hydrochloric Acid → Ethyl 4-(furan-2-yl)-2,4-dioxobutanoate

https://huagongshe.com/reaction/1250753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
Reactant2-AcetylfuranHCID 14505—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(furan-2-yl)-2,4-dioxobutanoateHCID 300675358.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of sodium hydride (5.4 g of 60% dispersion in mineral oil, 136 mmol, mineral oil was removed by washing twice with hexanes) in 100 mL of tetrahydrofuran at ambient temperature was added diethyl oxalate (12.3 mL, 91 mmol). To this mixture was added 2-acetylfuran (5.0 g, 45 mmol) as a solution in 25 mL of tetrahydrofuran. The resulting mixture was stirred at 70° C. for 1 h. The reaction was cooled to room temperature and then 10% HCl was added slowly until the solution was acidic. The tetrahydrofuran was removed in vacuo and the residue was taken up in ethyl acetate. The organics were washed with brine, dried (MgSO4) and concentrated to afford 5.5 g (58%) of the title compound which was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339099B1
Source datasetuspto-grants-2002_01
ORD IDord-11aeaa560a6e480f82e2721d57fdf261
Source noteuspto-grants-2002_01