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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(2-Methyl-1-phenylpropan-2-yl)-2-(propan-2-ylidene)hydrazine | HCID 86697459 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2-methyl-1-phenylpropan-2-yl)-3-phenyl-1H-pyrazol-5(4H)-one | HCID 86697458 | 50.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658686B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-3e74574aaa524983b53b69002256e7b7 |
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| Source note | uspto-grants-2014_02 |
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