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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670302Generated: October 25, 2026

Ethyl 2,4-dioxovalerate → 1-Benzyl-5-methyl-1h-pyrazole-3-carboxylate

https://huagongshe.com/reaction/1670302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2,4-dioxovalerateHCID 69208—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzylhydrazine dihydrochlorideHCID 146540—
SolventEthanolHCID 702—
Product1-Benzyl-5-methyl-1h-pyrazole-3-carboxylateHCID 1037600392.5%

Reaction Steps

To a solution of 1-benzylhydrazine dihydrochloride (Aldrich, 0.98 g, 5.0 mmol) in EtOH (30 mL) were added DIEA (2.0 mL) and ethyl 2,4-dioxopentanoate (0.70 mL, 5.0 mmol). The mixture was stirred at room temperature for 12 h and was concentrated in vacuo. The residue was dissolved in 1 N NaOH (10 mL). The solution was heated at 60° C. for 1 h. After cooling down, the solution was extracted with DCM (3×50 mL). The aqueous layer was neutralized to pH 2.0 and then was extracted with EtOAc. The organic layer was washed with brine and dried over MgSO4. It was filtered and concentrated to give 1-benzyl-5-methyl-1H-pyrazole-3-carboxylic acid (1.0 g, 92% yield). MS (ESI+): m/z 217.12 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989477B2
Source datasetuspto-grants-2011_08
ORD IDord-811dc588c8994990bfb39ac571eaa7a2
Source noteuspto-grants-2011_08