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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098591Generated: October 30, 2026

Ethanol → Ethyl 1-tert-butyl-5-methyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/1098591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
ReactantHCID 86623854HCID 86623854—
SolventDiethyl EtherHCID 3283—
ProductEthyl 1-tert-butyl-5-methyl-1H-pyrazole-3-carboxylateHCID 280055745%

Reaction Steps

In ethanol (5 mL) was placed the t-butylhydrazine hydrochloride (0.79 g, 6.3 mmol) and ethyl 2-acetyl-3-(dimethylaminomethylene)acrylate (1.0 g, 6.3 mmol). The mixture was refluxed for 8 hours. The mix was evaporated at reduced pressure to give an oil. The oil was dissolved in ether (25 mL) and washed successively with water (25 mL), saturated sodium bicarbonate (25 mL) and brine (25 mL) was dried (Na2SO4), concentrated in vacuo and purified by silica gel column chromatography (EtOAc/hexanes) to obtain ethyl 1-tert-butyl-5-methyl-1H-pyrazole-3-carboxylate (0.60 g, 45% yield). 1H NMR (400 MHz, DMSO-d6): δ 6.54 (s, 1H), 4.22 (q, J=7.2 Hz, 2H), 2.44 (s, 3H), 2.42 (s, 3H), 1.57 (s, 9H), 1.25 (t, J=7.2 Hz, 3H); MS (ESI) m/z: 211.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143293B2
Source datasetuspto-grants-2012_03
ORD IDord-2557e3d52995472496a22fc614158656
Source noteuspto-grants-2012_03