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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637548Erstellt: 25. Oktober 2026

Sodium Hydroxide → 3,3'-Diaminobenzophenone

https://huagongshe.com/reaction/637548

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt4,4'-Dichloro-3,3'-dinitrobenzophenoneHCID 348301—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3,3'-DiaminobenzophenoneHCID 69145—

Reaktionsschritte

To a closed glass vessel equipped with a thermometer and a stirrer, there are added 102 g (0.3 moles) of 3,3'-dinitro-4,4'-dichloro benzophenone, 5 g of 5% palladium/active carbon catalyst (available from Nihon Engelhardt Co.) and 300 ml of dioxane. While the mixture is being stirred at 70°-80° C., hydrogen is introduced in the vessel so that 41.5 l (1.85 moles) of hydrogen is absorbed into the mixture over 8 hours. After addition of 80 g (0.8 moles) of 40% aqueous sodium hydroxide, hydrogen is again introduced to the vessel with the mixture being stirred at 70°-80° C., so that it is absorbed 13.8 l (0.62 moles) over 3 hours. The reaction solution is filtered at 70°-80° C. to remove the catalyst. On cooling the solution, there is obtained 3,3'-diamino benzophenone, as yellow needle-like crystals. The crystals are filtered, washed with 30 ml of 50% aqueous solution of dioxane and dried. Yield 59.2 g (93%). M.P. 149°-151° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04556738
Quelldatensatzuspto-grants-1985_12
ORD IDord-e6ecfb5e17d74705ae657c0e1a1bbc07
Quellennotizuspto-grants-1985_12