HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19432844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1-Ethoxyethylidene)malononitrile | HCID 79450 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19432844 | HCID 19432844 | 98.3% |
Reaction Steps
A mixture of 1-ethoxyethylidene malononitrile (60.0 g, 0.4 mol), tert-butylhydrazine hydrochloride (50.0 g, 0.4 mol) and ethanol (500 ml) was heated to reflux. The heat was removed and triethylamine (55.8 ml, 0.4 mol) was added dropwise at such a rate as to maintain a gentle reflux. The reaction mixture was refluxed for an additional 1 hour, cooled to room temperature and the solvent was removed in vacuo. The residue was taken up in ethyl acetate (300 ml) and washed with water (200 ml). The organic layer was separated, washed with brine and dried over sodium sulfate. The solvent was removed in vacuo to afford 75.6 g (67%) of 1-tert-butyl-3-ethyl-5-amino-1H-pyrazole-4-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294612 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-03f1b082ab7344eab12a88fca0835b1e |
| Source note | uspto-grants-1994_03 |