HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37465Generated: October 26, 2026
Diethyl Oxalate → 2,4-Dioxo-4-phenyl-butyric acid ethyl ester
https://huagongshe.com/reaction/37465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,4-Dioxo-4-phenyl-butyric acid ethyl ester | HCID 226503 | — |
Reaction Steps
In 560 ml of ethanol was dissolved 25 g (1.08 eq.) of sodium and a mixture of 135.6ml (146 g; 1 mol) of diethyl oxalate and 116.7 ml (120 g; 1 mol) of acetophenone was added thereto dropwise at 40° C. One hour later, reflux was begun and it was continued for 30 minutes. The solvent was distilled off. The residue was neutralized with sulfuric acid (55 g/water 200 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. Thereafter, the solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent: dichloromethane/hexane 1:1), to give colorless plates. The crystals were recovered by filtration with ethyl acetate/hexane. Yield: 114.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420275 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-f711d3437ac74f85b47876be8d6e5fe7 |
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| Source note | uspto-grants-1995_05 |
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