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HRID 2286434作成日:2026年10月27日

Benzene → [1,1'-Biphenyl]-4,4'-diamine, N4,N4'-bis(3-methylphenyl)-N4,N4'-diphenyl-

https://huagongshe.com/reaction/2286434

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Dimethyl SulfoxideHCID 679—
反応物Potassium CarbonateHCID 11430—
反応物3-IodotolueneHCID 12268—
反応物N,N'-DiphenylbenzidineHCID 68280—
触媒CopperHCID 23978—
生成物[1,1'-Biphenyl]-4,4'-diamine, N4,N4'-bis(3-methylphenyl)-N4,N4'-diphenyl-HCID 103315—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04265990
出典データセットuspto-grants-1981_05
ORD IDord-e01a778db17d49b4987c72cd474f0549
出典メモuspto-grants-1981_05