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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896688Generated: November 3, 2026

Diethyl Oxalate → Ethyl 4-(furan-2-yl)-2,4-dioxobutanoate

https://huagongshe.com/reaction/1896688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant2-AcetylfuranHCID 14505—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductEthyl 4-(furan-2-yl)-2,4-dioxobutanoateHCID 3006753—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of sodium ethoxide (6.81 g) in absolute ethanol (200 mL). was slowly added 2-acetylfuran (5.01 mL) at 0° C. The resulting solution was stirred at 0° C. for 2 hours, and diethyl oxalate (9.30 mL) was slowly added to the solution. The resulting solution was stirred for 18 hours, and the reaction was quenched with 1N hydrochloric acid solution. The resulting mixture was concentrated under reduced pressure, and residue was then extracted with methylene chloride. An organic phase was dried over anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure to give 10.0 g of 4-furan-2-yl-2,4-dioxo-butyric acid ethyl ester. This concentrate was used in the next steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518978B2
Source datasetuspto-grants-2013_08
ORD IDord-96328210102d44c094770e0255a3e8de
Source noteuspto-grants-2013_08