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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (4-Chloro-3-nitrophenyl)(4-nitrophenyl)methanone | HCID 554735 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | (3-Aminophenyl)(4-aminophenyl)methanone | HCID 148536 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04556738 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-bf82a535b9324f8b89d93d378c8d5142 |
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| Source note | uspto-grants-1985_12 |
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