참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (2-Chloro-5-nitrophenyl)(4-chloro-3-nitrophenyl)methanone | HCID 230560 | — |
| 반응물 | Azane;hydrate | HCID 12896473 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 3,3'-Diaminobenzophenone | HCID 69145 | — |
반응 단계
In a closed glass vessel with a thermometer and a stirrer, there are charged 102.3 g (0.3 moles) of 2,4'-dichloro-5,3'-dinitro benzophenone, 5 g of 5% palladium/active carbon catalyst (from Nihon-Engelhardt Co.) and 300 ml of dioxane. At 70°-80° C., hydrogen is introduced into the vessel while the mixture being stirred, so that 42 l (1.88 moles) of hydrogen is absorbed in the mixture during ten hours. After being cooled to 30° C., the mixture is added with 55 g (0.9 moles) of 28% ammonia water and then introduced with hydrogen while being stirred at 30°-40° C. so as to absorb 13.2 l (0.59 moles) of hydrogen during 5 hours. The reaction mixture is subject to filtering at 30°-40° C. to remove the catalyst. On cooling, there is obtained 3,3'-diamino benzophenone as yellow crystals. The crystals are filtered, washed with 30 ml of 50% aqueous solution of dioxane and dried. Yield 56.5 g (89%). M.P. 149°-150.5° C. Recrystallization from ethanol gives yellow needle-like pure crystals of said benzophenone. 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-7c2c2d1a711c48e4859820b5212da161 |
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| 출처 메모 | uspto-grants-1985_12 |
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