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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491851Generated: October 26, 2026

Ethyl 2-formyl-3-oxopropanoate → 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/491851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-formyl-3-oxopropanoateHCID 11029955—
Reactant3-Hydrazino-4-methylbenzoic acid hydrochlorideHCID 56777508—
SolventEthanolHCID 702—
Product1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 5755970868%

Reaction Steps

A solution of 2-formyl-3-oxo-propionic acid ethyl ester (S. H. Bertz et al., J. Org. Chem., 1982, 47, 2216) (1.44 g, 10 mmol) in EtOH (10 mL) was cooled in an ice bath. A slurry of 3-hydrazino-4-methyl-benzoic acid hydrochloride (2.02 g, 10 mmol) in EtOH (50 mL) was added and the reaction was stirred overnight. The EtOH was removed under reduced pressure and the residue partitioned between water and CH2Cl2. The layers were separated and the organic layer washed with brine. The organic layer was dried over Na2SO4, filtered, and concentrated. Hexanes were added and the solution concentrated. The resulting solid was collected by vacuum filtration, washed with hexanes and dried under vacuum to provide 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester (1.86 g, 68%) as a yellow solid: ESI MS m/z 275 [C14H14N2O4+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531560B2
Source datasetuspto-grants-2009_05
ORD IDord-c22620a1782542e7943f04f163d8a864
Source noteuspto-grants-2009_05