HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Ethoxyethylidene)malononitrile → 5-Amino-3-methyl-1-(tetrahydro-3-furanyl)-1H-pyrazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Ethoxyethylidene)malononitrile | HCID 79450 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (Tetrahydrofuran-3-yl)hydrazine hydrochloride | HCID 19432761 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-3-methyl-1-(tetrahydro-3-furanyl)-1H-pyrazole-4-carbonitrile | HCID 19432818 | 54.3% |
Reaction Steps
A mixture of 3-tetrahydrofuranylhydrazine hydrochloride (6.2 g, 0.045 mol), sodium methoxide (2.4 g, 0.045 mol) and ethanol (70 ml) was refluxed under argon for 10 minutes. The reaction mixture was cooled to room temperature and 1-ethoxyethylidene malononitrile (6.1 g, 0.045 mol) was added. The reaction mixture was heated to reflux and stirred for 21 hours. The reaction was cooled and the solvent was removed in vacuo. The residue was recrystallized from water to afford 4.7 g (54%) of 1-(3-tetrahydrofuranyl)-3-methyl-5-amino-1H-pyrazole-4-carbonitrile as yellow crystals, m.p. 134°-135° C. when dried at 90° C. in high vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294612 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-e19d10f830884bab940067d8f90c9196 |
| Source note | uspto-grants-1994_03 |