참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 3-Iodotoluene | HCID 12268 | — |
| 반응물 | N,N'-Diphenylbenzidine | HCID 68280 | — |
| 촉매 | Copper | HCID 23978 | — |
| 생성물 | [1,1'-Biphenyl]-4,4'-diamine, N4,N4'-bis(3-methylphenyl)-N4,N4'-diphenyl- | HCID 103315 | — |
반응 단계
In a 5000 milliliter, round bottom, 3 necked flask fitted with a mechanical stirrer and blanketed with argon, is placed 336 grams (1 mole) of N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine, 550 grams (2.5 moles) of m-iodotoluene, 550 grams (4 moles) potassium carbonate (anhydrous) and 50 grams of copper bronze catalyst and 1500 ml dimethylsulfoxide (anhydrous). The heterogeneous mixture is refluxed for 6 days. The mixture is allowed to cool. 2000 ml of benzene is added. The dark slurry is then filtered. The filtrate is extracted 4 times with water. Then the filtrate is dried with magnesium sulfate and filtered. The benzene is taken off under reduced pressure. The black product is column chromatographed using Woelm neutral alumina. Colorless crystals of the product are obtained by recrystallizing the product from n-octane. The melting point is 167°-169° C. The yield is 360 grams (65%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04346158 |
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| 출처 데이터셋 | uspto-grants-1982_08 |
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| ORD ID | ord-86a6dc0eacb141b18be93852b04c1774 |
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| 출처 메모 | uspto-grants-1982_08 |
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