HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429291Generated: October 27, 2026
Hydrazine hydrate (1:1) → ethyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetate
https://huagongshe.com/reaction/1429291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Ethyl 3-acetyl-4-oxopentanoate | HCID 87820 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetate | HCID 16394806 | 72% |
Reaction Steps
To a solution of ethyl 3-acetyl-4-oxopentanoate (synthesized as described D. P. Shrout and D. A. Lightner, Synth. Commun. 20 (1990), 2075) (9.676 g, 51.96 mmol) in ethanol, at 0° C., was added slowly a solution of hydrazine hydrate (2.990 g, 59.75 g) in absolute ethanol. The reaction mixture was warmed to room temperature and stirred for 2 hours. After removing ethanol under vacuum, dichloromethane and water were added to the crude product and the organic layer was separated. The aqueous layer was extracted further with dichloromethane and the combined organic extracts were washed with water. After drying over MgSO4 and evaporation of the solvent under reduced pressure, the pyrazole was isolated as a yellow oil. Yield: 72% (6.777 g, 37.2 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940273B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-b45de8d21d7240b89b097fb18bed1f1b |
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| Source note | uspto-grants-2015_01 |
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