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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736570Generated: November 3, 2026

2-(Ethoxymethylene)propanedinitrile → 5-amino-1-tert-butyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1736570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethoxymethylene)propanedinitrileHCID 67152—
Reactanttert-ButylhydrazineHCID 81890—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
Product5-amino-1-tert-butyl-1H-pyrazole-4-carbonitrileHCID 279745487.5%

Reaction Steps

To a mixture of tert-butylhydrazine (40 g, 0.32 mol), sodium methoxide (18 g, 0.32 mol) and ethanol 150 ml) was added ethoxymethylene malononitrile (42 g, 0.32 mol). The reaction mixture was heated to reflux for 2 hours and the solvent was removed in vacuo. The residue was extracted with chloroform, washed with water and the organic layer was concentrated in vacuo to afford 46 g (87%) of 1-tert-butyl-5-amino-1H-pyrazole-4-carbonitrile as a semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541187
Source datasetuspto-grants-1996_07
ORD IDord-c815d297dd404e33ac24f2dffda46db9
Source noteuspto-grants-1996_07