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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylacetateHCID 7170—
ReactantEthyl AcetateHCID 8857—
Reactant2-Bromo-1-cyclohexylethanoneHCID 11160027—
SolventSodium chloride; waterHCID 57417360—
Product2-Benzoyl-4-cyclohexyl-4-oxo-butyric acid ethyl esterHCID 57423724100%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488832B2
Source datasetuspto-grants-2009_02
ORD IDord-5fa9e58dde6b498a8e0f733cb2695fe6
Source noteuspto-grants-2009_02