HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240805Generated: October 25, 2026
Ethyl Acetoacetate → Ethyl 5-methyl-1-phenyl-1H-pyrazole-4-carboxylate
https://huagongshe.com/reaction/240805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Phenylhydrazine hydrochloride | HCID 60962 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-methyl-1-phenyl-1H-pyrazole-4-carboxylate | HCID 96680 | 87.6% |
Reaction Steps
A mixture of ethyl acetoacetate (1.5 g, 11.5 mmol) and dimethylformamide dimethyl acetal (1.68 mL, 12.7 mmol) was stirred at 120° C. for 2 hours. The reaction solution was cooled to room temperature, and a solution of phenyl hydrazine hydrochloride (1.67 g, 11.5 mmol) in ethanol (30 mL) was then added thereto. The obtained mixture was stirred at 80° C. for 2.5 hours. The reaction solution was cooled to room temperature, and it was then concentrated under reduced pressure. The residue was purified with a fractionation purification apparatus (Biotage, ethyl acetate:hexane=1:19-3:7), so as to obtain the title compound (2.32 g, 87%) in the form of a yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648103B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-56649bbc9a974d688e5688716682c800 |
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| Source note | uspto-grants-2014_02 |
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