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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132509생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/132509

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Sodium CarbonateHCID 10340—
반응물9,10-DibromoanthraceneHCID 68226—
반응물[4-[Bis(4-methylphenyl)amino]phenyl]boronic acidHCID 23083792—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물9-[Bis(4-methylphenyl)amino]phenyl-10-bromoanthraceneHCID 86601349—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07387845B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-54ef8cedab1c4634807a5cf24457e021
출처 메모uspto-grants-2008_06