HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-(4-Aminophenyl)pyrazin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 5-(4-Nitrophenyl)pyrazin-2(1H)-one | HCID 13853573 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(4-Aminophenyl)pyrazin-2(1H)-one | HCID 12358028 | 81.2% |
Reaction Steps
5-(4-Nitrophenyl)-2(1H)-pyrazinone (0.1 g) was warmed with water (2.5 ml) and 1N sodium hydroxide solution (0.46 ml) to about 70° C. To this solution was added 10% Palladium on charcoal (0.01 g), and subsequently hydrazine hydrate (0.1 ml). The well-stirred mixture was heated for 2 minutes, stirred for a further 2 minutes and filtered whilst hot. The filtrate was taken to pH6 with dilute hydrochloric acid, whereupon the solid was collected by filtration, washed with water and dried to give 5-(4-aminophenyl)-2(1H)-pyrazinone (0.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04657906 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-b3e6d0bfa3eb4ffc9b418ef8e88ae029 |
| Source note | uspto-grants-1987_04 |