참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4,4'-Dichloro-3,3'-dinitrobenzophenone | HCID 348301 | — |
| 반응물 | Calciumoxide | HCID 6850728 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 3,3'-Diaminobenzophenone | HCID 69145 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04556738 |
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| 출처 데이터셋 | uspto-grants-1985_12 |
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| ORD ID | ord-320100a0c75c4b7296d3cb6866d9835d |
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| 출처 메모 | uspto-grants-1985_12 |
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