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HRID 600118作成日:2026年10月26日

Dodecane → N4,N4-di([1,1'-biphenyl]-4-yl)-N4'-phenyl-[1,1'-biphenyl]-4,4'-diamine

https://huagongshe.com/reaction/600118

反応式

関与物質

役割名称HCID仕込み量
反応物DodecaneHCID 8182—
反応物Potassium CarbonateHCID 11430—
反応物Potassium HydroxideHCID 14797—
反応物Bis-biphenyl-4-yl-amineHCID 504244—
反応物N-(4'-iodobiphenylyl)acetanilideHCID 23140821—
触媒CopperHCID 23978—
溶媒WaterHCID 962—
溶媒Isoamyl AlcoholHCID 31260—
生成物N4,N4-di([1,1'-biphenyl]-4-yl)-N4'-phenyl-[1,1'-biphenyl]-4,4'-diamineHCID 2314081969.9%

反応手順

There were mixed 20.70 g (0.050 mole) of N-(4′-iodobiphenylyl)acetanilide, 19.95 g (0.060 mole) of N,N-bis(biphenyl-4-yl)amine, 10.40 g (0.075 mole) of anhydrous potassium carbonate, 0.20 g (0.003 mole) of copper powder and 10 ml of n-dodecane, followed by reaction at 200 to 212° C. for 15 hours. The reaction product was extracted with 200 ml of toluene, and the insoluble matter was removed by filtration. Then, the filtrate was concentrated to obtain crude crystals. The crude crystals were dissolved in 80 ml of isoamyl alcohol, and 5 ml of water and 5.00 g (0.075 mole) of 85% potassium hydroxide were added, followed by hydrolysis at 130° C. After isoamyl alcohol was removed by steam distillation, extraction with 250 ml of toluene was performed, and the organic layer was washed with water, dried and concentrated. The concentrate was purified by column chromatography (carrier: silica gel, eluate: toluene/n-hexane=1/2) to obtain 24.2 g (yield: 69.9%, HPLC purity: 98.0%) of N,N-bis(biphenyl-4-yl)-N′-phenyl-4,4′-diaminobiphenyl. The melting point was 145.8 to 146.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07897816B2
出典データセットuspto-grants-2011_03
ORD IDord-71c0a2f7086e482a881ab9f8dc376607
出典メモuspto-grants-2011_03