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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599313Generated: October 29, 2026

Ethanol → ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/599313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
Reactant(Dimethylaminomethylene)-3-oxobutanoateHCID 86629460—
SolventDiethyl EtherHCID 3283—
Productethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylateHCID 1365417765%

Reaction Steps

In ethanol (10 mL) was placed the tert-butylhydrazine hydrochloride (1.35 g, 10.8 mmol) and ethyl 2-((dimethylaminomethylene)-3-oxobutanoate (2.00 g, 10.8 mmol). The mixture warmed to reflux and stirred for 2 hrs, cooled to RT and stirred overnight. The mixture was evaporated at reduced pressure to give an oil which was dissolved in ether (25 mL) and washed successively with water (25 mL), saturated sodium bicarbonate (25 mL) and brine (25 mL), dried (Na2SO4 and evaporated at reduced pressure to give an oil. The oil was purified by chromatography (Biotage S1-25 column, 10-40% ethyl acetate/Hex 750 mL) to give ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate (1.48 g, 65% yield) as an oil. MS (ESI) m/z: 211.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897762B2
Source datasetuspto-grants-2011_03
ORD IDord-5676cb8321db4570b4f15d2f6209e294
Source noteuspto-grants-2011_03