HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-enenitrile → 1-(3-Chlorophenyl)-5-phenyl-4,5-dihydro-1h-pyrazol-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-enenitrile | HCID 74667 | — |
| Reactant | (3-Chlorophenyl)hydrazine | HCID 75332 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-Chlorophenyl)-5-phenyl-4,5-dihydro-1h-pyrazol-3-amine | HCID 13309514 | — |
Reaction Steps
A 0.6 g. amount of sodium metal is dissolved in 100 ml. of absolute ethanol, then 14.76 g. of m-chlorophenylhydrazine is added followed in 5 minutes by 12.92 g. of cinnamonitrile. The reaction mixture is refluxed for 6 hours, then cooled in an ice-bath. The precipitate formed is collected by filtration, then is dissolved in dichloromethane. This solution is passed through a short column of a hydrous magnesium silicate. The effluent is heated to reflux on a steam bath and hexane is added until a precipitate occurs. The product is collected, then is recrystallized from dichloromethane-hexane to give 7.55 g. of the product of the Example as salmon colored needles, m.p. 164°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451479 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-26a48b3f007b48fbb6cc0336caf40ab4 |
| Source note | uspto-grants-1984_05 |