HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725189Generated: October 27, 2026
Ethyl benzoylacetate → 2-Benzoyl-4-cyclohexyl-4-oxo-butyric acid ethyl ester
https://huagongshe.com/reaction/1725189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Bromo-1-cyclohexylethanone | HCID 11160027 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Benzoyl-4-cyclohexyl-4-oxo-butyric acid ethyl ester | HCID 57423724 | 100% |
Reaction Steps
To a stirred slurry of 1.44 g (36 mmol) sodium hydride, obtained as a 60% dispersion in mineral oil, in 45 mL anhydrous THF, at 0° C., was added dropwise 6.48 g (33.75 mmol) ethyl benzoyl acetate. The resulting slurry was stirred at 0° C. for 0.5 hr, upon which time was added dropwise the entire sample of 2-bromo-1-cyclohexyl-ethanone obtained in Step 1. The reaction was stirred at room temperature for 24 hr and poured into 0.4 L brine. The brine was shaken with ethyl acetate twice and the combined organic extracts were dried over MgSO4 and concentrated to afford 14.37 g (45.4 mmol, >100% yield) of 2-benzoyl-4-cyclohexyl-4-oxo-butyric acid ethyl ester. The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488832B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-5fa9e58dde6b498a8e0f733cb2695fe6 |
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| Source note | uspto-grants-2009_02 |
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