HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773773Generated: October 26, 2026
Diethyl Oxalate → 2,4-Dioxo-5-phenoxy-pentanoic acid ethyl ester
https://huagongshe.com/reaction/1773773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1-Phenoxy-2-propanone | HCID 69313 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,4-Dioxo-5-phenoxy-pentanoic acid ethyl ester | HCID 57435086 | 54% |
Reaction Steps
Sodium (6.74 g, 293 mmol) was added to EtOH (808 mL) at 0° C. The mixture was stirred at 0° C. until the sodium was completely dissolved. Then phenoxy-2-propanone (53 mL, 266 mmol) was added dropwise. The mixture was stirred at 0° C. for 10 minutes and then diethyl oxalate (36 mL, 266 mmol) was added. Then the mixture was stirred at room temperature for 16 hours and the solvent was evaporated in vacuo. The residue was dissolved in H2O and the mixture was acidified with a 1M solution of HCl and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo. The crude product was purified by open column chromatography (silica; DCM) to yield 2,4-dioxo-5-phenoxy-pentanoic acid ethyl ester (35.9 g, 54% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255103B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-b8195e39ee5a45ee81fc19b7f782f4a6 |
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| Source note | uspto-grants-2016_02 |
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