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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637549Erstellt: 25. Oktober 2026

Benzene → 3,3'-Diaminobenzophenone

https://huagongshe.com/reaction/637549

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktPotassium CarbonateHCID 11430—
Edukt3,3'-Dinitro-4-chloro-4'-fluoro benzophenoneHCID 22987185—
EduktHCID 178418361HCID 178418361—
KatalysatorTrioctylmethylammonium chlorideHCID 21218—
KatalysatorPalladiumHCID 23938—
LösungsmittelHydrochloric AcidHCID 313—
Produkt3,3'-DiaminobenzophenoneHCID 69145104,3%

Reaktionsschritte

To a closed glass vessel equipped with a thermometer and a stirrer, there are added 49 g (0.15 moles) of 3,3'-dinitro-4-chloro-4'-fluoro benzophenone, 1 g of palladium black catalyst and 300 ml of benzene. While the mixture being stirred at 65°-70° C., 20.2 l (0.9 moles) of hydrogen is absorbed therein during about 6 hours. Then, after there are added 180 g (0.45 moles) of 35% aqueous solution of potassium carbonate and 3 g of 90% aqueous solution of trioctylmethyl ammonium chloride (available from Tokyo-Kasei Co.), additional hydrogen, 7.4 l (0.33 moles), is introduced during about 5 hours while the mixture being stirred at 65°-70° C. The mixture at that temperature is filtered to remove the catalyst. Organic phase is separated from the filtrate, added with magnesium sulfate for removing water and then blown with dry hydrochloric gas to saturation. The precipitate thus obtained is filtered, washed with 50 ml of benzene and dried to obtain 33.2 g (yield 77.7%) of 3,3'-diamino benzophenone in the hydrochloric acid salt form. Recrystallization from 20% aqueous isopropyl alcohol gives pure compound, as slightly yellow needle-like crystals. M.P. 265°-267° C. (decomposed).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04556738
Quelldatensatzuspto-grants-1985_12
ORD IDord-04b3a5dbfc8645a28e4e89f16160a1f7
Quellennotizuspto-grants-1985_12