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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,4'-Dichloro-3,3'-dinitrobenzophenone | HCID 348301 | — |
| Reactant | Calciumoxide | HCID 6850728 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3,3'-Diaminobenzophenone | HCID 69145 | — |
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
| 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-320100a0c75c4b7296d3cb6866d9835d |
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| Source note | uspto-grants-1985_12 |
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