HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637552Erstellt: 25. Oktober 2026
Azane;hydrate → (3-Aminophenyl)(4-aminophenyl)methanone
https://huagongshe.com/reaction/637552
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Azane;hydrate | HCID 12896473 | — |
| Edukt | 4-Bromo-3,4'-dinitro benzophenone | HCID 19708183 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | (3-Aminophenyl)(4-aminophenyl)methanone | HCID 148536 | — |
Reaktionsschritte
In a closed vessel equipped with a thermometer and a stirrer there are charged 105 g (0.3 moles) of 4-bromo-3,4'-dinitro benzophenone, 5 g of 5% palladium/active carbon catalyst (from Nihon-Engelhardt Co.) and 300 ml of dioxane. At 70°-80° C., with the mixture being stirred, there is introduced 41 l (1.83 moles) of hydrogen so as to be absorbed in the mixture in about 11 hours. Following cooling the mixture to 30° C., there is added 38.5 g (0.33 moles) of 30% ammonia water. Then, again with the mixture being stirred, at 30°-40° C., there is introduced an additional amount of hydrogen, 7.2 l (0.32 moles), during seven hours. The reaction liquid is filtered at 30°-40° C. to remove the catalyst and then allowed to cool giving yellow crystals of 3,4'-diamino benzophenone. The crystals are filtered, washed with 30 ml of 50% aqueous dioxane solution and dried. Yield 58 g (91%). M.P. 121°-123° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04556738 |
|---|
| Quelldatensatz | uspto-grants-1985_12 |
|---|
| ORD ID | ord-d9d6e48ed041483793cece1ab1cd589c |
|---|
| Quellennotiz | uspto-grants-1985_12 |
|---|