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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132509Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/132509

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
Edukt9,10-DibromoanthraceneHCID 68226—
Edukt[4-[Bis(4-methylphenyl)amino]phenyl]boronic acidHCID 23083792—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt9-[Bis(4-methylphenyl)amino]phenyl-10-bromoanthraceneHCID 86601349—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07387845B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-54ef8cedab1c4634807a5cf24457e021
Quellennotizuspto-grants-2008_06