HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazinecarboxaldehyde, 2-(4-nitrophenyl)- → Hydrazinecarboxaldehyde, 2-(4-aminophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazinecarboxaldehyde, 2-(4-nitrophenyl)- | HCID 5008489 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Hydrazinecarboxaldehyde, 2-(4-aminophenyl)- | HCID 113189 | 81.9% |
Reaction Steps
Then, 30 g of 1-formyl-2-(4-nitrophenyl)hydrazine was catalytically reduced in 1.6 liters of ethanol at room temperature using palladium-carbon as a catalyst. The reaction mixture was filtered to remove the catalyst and the filtrate was evaporated to dryness to provide 20.5 g of 1-formyl-2-(4-aminophenyl)hydrazine having a melting point of 123°-125° C. as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737452 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-7d946c2d603649f39489bd0293d466a3 |
| Source note | uspto-grants-1988_04 |