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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 2-Acetylfuran | HCID 14505 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(furan-2-yl)-2,4-dioxobutanoate | HCID 3006753 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518978B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-96328210102d44c094770e0255a3e8de |
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| Source note | uspto-grants-2013_08 |
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