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HRID 132509作成日:2026年10月27日

Toluene → 9-[Bis(4-methylphenyl)amino]phenyl-10-bromoanthracene

https://huagongshe.com/reaction/132509

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物9,10-DibromoanthraceneHCID 68226—
反応物[4-[Bis(4-methylphenyl)amino]phenyl]boronic acidHCID 23083792—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物9-[Bis(4-methylphenyl)amino]phenyl-10-bromoanthraceneHCID 86601349—

反応条件

温度80 °C

反応手順

In a nitrogen flow, 1 g (2.98 mmol) of 9,10-dibromoanthracene and 1.44 g (4.46 mmol) of bis(4-methylphenyl)aminobenzene-4-boronic acid were dissolved and stirred in a deaerated mixture solvent of 100 ml of toluene and 50 ml of ethanol, followed by dropping a sodium carbonate aqueous solution prepared by dissolving 9 g of anhydrous sodium carbonate in 45 ml of water. After stirring the mixture for 30 minutes, 257 mg (0.223 mmol) of tetrakis(triphenylphosphine)palladium was added thereto. Then, the mixture was heated and stirred for about 3 hours in an oil bath heated at 80° C. After returning the reaction solution to room temperature, 40 ml of water and 50 ml of ethyl acetate were added thereto and the resultant solution was then separated into an aqueous layer and an organic layer. Furthermore, the aqueous layer was extracted with toluene and ethyl acetate, and was then combined with the previous organic layer and dried with magnesium sulfate. The solvent was evaporated and then the residue was purified by silicagel-column chromatography (toluene:hexane=1:2) to obtain 1.13 g of 9-[bis(4-methylphenyl)amino]phenyl-10-bromoanthracene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07387845B2
出典データセットuspto-grants-2008_06
ORD IDord-54ef8cedab1c4634807a5cf24457e021
出典メモuspto-grants-2008_06