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
In 1,600 ml of ethanol, 30 g of 2-(4-nitrophenyl)-1-formylhydrazine was catalytically reduced at room temperature, using palladium-carbon as a catalyst. The reaction mixture was filtered and the filtrate was evaporated to dryness, whereby 20.5 g of white solid 2-(4-aminophenyl)-1-formylhydrazine was obtained. Melting point: 123° to 125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04323643 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-492ae1755ce34bd7b6473490bef01514 |
| Source note | uspto-grants-1982_04 |