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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244936Generated: October 31, 2026

Ethyl benzoylacetate → 1-(2-methyl-1-phenylpropan-2-yl)-3-phenyl-1H-pyrazol-5(4H)-one

https://huagongshe.com/reaction/244936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylacetateHCID 7170—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2-Methyl-1-phenylpropan-2-yl)-2-(propan-2-ylidene)hydrazineHCID 86697459—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product1-(2-methyl-1-phenylpropan-2-yl)-3-phenyl-1H-pyrazol-5(4H)-oneHCID 8669745850.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

500 mg (2.45 mmol) of 1-(2-methyl-1-phenylpropan-2-yl)-2-(propan-2-ylidene)hydrazine was dissolved in 3.0 mL of glacial acetic acid, mixed with 429 mg (2.23 mmol) of ethyl 3-oxo-3-phenylpropanoate and stirred at 100° C. for 4 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate, neutralized with saturated aqueous sodium hydrogen carbonate (100 ml) and extracted with ethyl acetate. The resulting organic layer was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography using hexane-ethyl acetate (100:1 to 9:1) as the eluent to give 330 mg of the desired product as a pale orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658686B2
Source datasetuspto-grants-2014_02
ORD IDord-3e74574aaa524983b53b69002256e7b7
Source noteuspto-grants-2014_02