HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487242Generated: October 29, 2026
(1-Ethoxyethylidene)malononitrile → HCID 19432763, compound
https://huagongshe.com/reaction/487242
Participants
| Role | Name | HCID | Charge |
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| Reactant | (1-Ethoxyethylidene)malononitrile | HCID 79450 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 19432785 | HCID 19432785 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19432763 | HCID 19432763 | 56.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05294612 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-c73d3c9944d343abb31e5e54d02e6a60 |
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| Source note | uspto-grants-1994_03 |
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