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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570071Generated: October 27, 2026

Hydrazine hydrate (1:1) → ethyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetate

https://huagongshe.com/reaction/570071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantEthyl 3-acetyl-4-oxopentanoateHCID 87820—
SolventEthanolHCID 702—
Productethyl 2-(3,5-dimethyl-1H-pyrazol-4-yl)acetateHCID 1639480672%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023315B2
Source datasetuspto-grants-2015_05
ORD IDord-6a8f0cd3400541e4857ea3b52f549c08
Source noteuspto-grants-2015_05