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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098555Generated: November 1, 2026

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

https://huagongshe.com/reaction/1098555

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
ReactantEthyl 2-acetyl-3-(dimethylamino)acrylateHCID 3806790—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Productethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylateHCID 1365417765.2%

Reaction Steps

In ethanol (10 mL) was placed the tert-butylhydrazine hydrochloride (1.35 g, 10.8 mmol) and ethyl 2-((dimethylamino)methylene)-3-oxobutanoate (2.00 g, 10.8 mmol). The mixture warmed to reflux and stirred for 2 hrs, then 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), evaporated at reduced pressure and purified by chromatography (S1-25 column, ethyl acetate/hexanes) 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 numberUS08143293B2
Source datasetuspto-grants-2012_03
ORD IDord-5a0da16277ae4adc88e09523447fa3da
Source noteuspto-grants-2012_03