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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637547Generated: October 25, 2026

4,4'-Dichloro-3,3'-dinitrobenzophenone → 3,3'-Diaminobenzophenone

https://huagongshe.com/reaction/637547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4'-Dichloro-3,3'-dinitrobenzophenoneHCID 348301—
ReactantCalciumoxideHCID 6850728—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,2-DichloroethaneHCID 11—
Product3,3'-DiaminobenzophenoneHCID 69145—

Reaction Conditions

Temperature70 °C

Reaction Steps

To an autoclave there are added 50 g (0.15 moles) of 3,3'-dinitro-4,4'-dichloro benzophenone, 21 g (0.38 moles) of calcium oxide, 1 g of 5% palladium/alumina catalyst (available from Nihon-Engelhardt Co., Ltd.) and 350 ml of 1,2-dichloro ethane. The reaction is carried out for ten hours by introducing hydrogen into the autoclave, with the mixture being stirred at 30°-35° C., to keep the pressure at 10 Kg/cm2.G. After the completion of the reaction, the reaction mixture is heated up to 70° C. and subjected to a hot filtering so as to remove the catalyst and the inorganic salt. On cooling the mixture there are obtained yellow needle-like crystals of 3,3'-diamino benzophenone. The crystals are filtered, washed with 10 ml of 1,2-dichloro ethane and dried. Yield 21.2 g (67%). M.P. 149°-150.5° C. Recrystallization from ethanol gives pure crystals. M.P. 150°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556738
Source datasetuspto-grants-1985_12
ORD IDord-320100a0c75c4b7296d3cb6866d9835d
Source noteuspto-grants-1985_12