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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487242Generated: October 29, 2026

(1-Ethoxyethylidene)malononitrile → HCID 19432763, compound

https://huagongshe.com/reaction/487242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Ethoxyethylidene)malononitrileHCID 79450—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 19432785HCID 19432785—
SolventEthanolHCID 702—
ProductHCID 19432763HCID 1943276356.2%

Reaction Steps

To a solution of 2-methylcyclopentylhydrazine hydrochloride (7.4 g, 48.8 mmol) in ethanol (100 ml) was added sodium methoxide (2.6 g, 48.8 mmol). The resulting white suspension was stirred for 10 minutes at room temperature and then (1-ethoxyethylidene)malononitrile (6.7 g, 48.8 mmol) was added. The reaction mixture was heated to reflux and was stirred for 5 hours. The solvent was removed in vacuo and the residue was partitioned between chloroform and water. The organic layer was separated and the aqueous layer was extracted with chloroform three times. The combined organic layers were washed with brine, then dried over anhydrous MgSO4. The solution was passed through a plug of silica gel and the solvent was removed in vacuo. The residue was washed with ether to afford 5.6 g (56%) of 1-(2-methylcyclopentyl)-3-methyl-5-amino-1H-pyrazole-4-carbonitrile as a white powder, m.p. 158°-159° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294612
Source datasetuspto-grants-1994_03
ORD IDord-c73d3c9944d343abb31e5e54d02e6a60
Source noteuspto-grants-1994_03