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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637554Generated: October 25, 2026

Sodium Carbonate → (3-Aminophenyl)(4-aminophenyl)methanone

https://huagongshe.com/reaction/637554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(4-Chloro-3-nitrophenyl)(4-nitrophenyl)methanoneHCID 554735—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,2-DichloroethaneHCID 11—
Product(3-Aminophenyl)(4-aminophenyl)methanoneHCID 148536—

Reaction Conditions

Temperature70 °C

Reaction Steps

To an autoclave there are added 30.7 g (0.1 moles) of 4-chloro-3,4'-dinitro benzophenone, 10.6 g (0.1 moles) of sodium carbonate, 1 g of 5% palladium/alumina catalyst (available from Nihon-Engelhardt Co.) and 250 ml of 1,2-dichloro ethane. With the mixture being stirred at 30°-35° C., the reaction is carried out at a constant pressure for 10 hours by introducing hydrogen into the mixture. After completion of the reaction, the reaction mixture is heated up to 70° C. to be subjected to filtering for removing the catalyst. Then, on cooling, there is obtained 3,4'-diamino benzophenone in the form of yellow needle-like crystals. The crystals are filtered, washed with 20 ml of 1,2-dichloro ethane and dried. Yield 17.6 g (83%). M.P. 121°-122° C. Recrystallization from ethanol gives yellow needle-like pure crystals of said benzophenone. M.P. 122°-122.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556738
Source datasetuspto-grants-1985_12
ORD IDord-bf82a535b9324f8b89d93d378c8d5142
Source noteuspto-grants-1985_12