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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748427Generated: October 26, 2026

Ethanol → 5-methyl-1-(4-methylphenyl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1748427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Methylphenylhydrazine monohydrochlorideHCID 12504—
ReactantSodium HydroxideHCID 14798—
ReactantButanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl esterHCID 97734—
SolventWaterHCID 962—
Product5-methyl-1-(4-methylphenyl)-1H-pyrazole-4-carboxylic acidHCID 276958357.7%

Reaction Steps

To an ethanol (70 ml) and water (70 ml) solution of ethyl 2-(ethoxymethylene)acetoacetate (16.67 g) prepared according to a method described in J. Chem. Soc. Perkin trans. I, 1875 (1988), was added 4-methylphenylhydrazine hydrochloride (14.2 g) and the mixture was stirred at reflux temperature for 7.5 hours. Sodium hydroxide (8.5 g) was added and the mixture was further stirred at reflux temperature for an hour. After completion of the reaction, the solvent was evaporated, diluted hydrochloric acid was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was washed with n-hexane to give the titled compound (11.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-c3f3e42018a94d56a631b599971ca2e4
Source noteuspto-grants-2015_10