HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-Enal → HCID 5130700, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-Enal | HCID 307 | — |
| Reactant | N-methyl-N-phenyl-hydrazine | HCID 36299 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 5130700 | HCID 5130700 | — |
Reaction Steps
6.6 g of cinnamaldehyde and 6.1 g of 1-methyl-1-phenylhydrazine were added to 50 ml of ethanol. To the mixture, two or three drops of 1 N hydrochloric acid were added. The mixture was heated and refluxed for about one hour. The reaction mixture was cooled and the crystals then separated, which were then collected on a suction funnel. The thus obtained crude cinnamaldehyde 1-methyl-1-phenylhydrazone was recrystallized from ethanol. The yield was 6.8 g (57.6%) of light yellow needle-like crystals which melt at 113.5°-114.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04332948 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-ac0f37fe07e14c7c9052533f20f2560e |
| Source note | uspto-grants-1982_06 |