HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534088Generated: October 27, 2026
Benzoic Acid → 3-(Benzoyloxy)-2,4-pentanedione
https://huagongshe.com/reaction/534088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Chloro-2,4-pentanedione | HCID 74328 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Benzoyloxy)-2,4-pentanedione | HCID 20738 | 96.12% |
Reaction Steps
A flask was charged with powdered potassium hydroxide (21.89 g, 390.2 mmol), benzoic acid (47.65 g, 390.2 mmol), and DMF (500 mL) was added. The mixture was heated at 50° C. for 1 hour. 3-Chloropentane-2,4-dione (52.5 g, 390.2 mmol) was added and the reaction was stirred at 50° C. overnight. The reaction was cooled to ambient temperature, diluted in water (1.5 L) and extracted with ether (3×500 mL). The combined organic layers were washed with water, saturated NH4Cl and brine. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford 2,4-dioxopentan-3-yl benzoate (82.59 g, 96.12% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853409B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-80a427b546934ca1b4d36365787bb86f |
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| Source note | uspto-grants-2014_10 |
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