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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637552Erstellt: 25. Oktober 2026

Azane;hydrate → (3-Aminophenyl)(4-aminophenyl)methanone

https://huagongshe.com/reaction/637552

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzane;hydrateHCID 12896473—
Edukt4-Bromo-3,4'-dinitro benzophenoneHCID 19708183—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(3-Aminophenyl)(4-aminophenyl)methanoneHCID 148536—

Reaktionsbedingungen

Temperatur30 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04556738
Quelldatensatzuspto-grants-1985_12
ORD IDord-d9d6e48ed041483793cece1ab1cd589c
Quellennotizuspto-grants-1985_12