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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1358109Erstellt: 27. Oktober 2026

Toluene → 2-(4-Diphenylaminophenyl)-1,4-bis(acetyloxymethyl)benzene

https://huagongshe.com/reaction/1358109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
EduktDiphenyl-(4-(4,4,5,5-tetramethyl-(1,3,2)dioxaborolan-2-yl)-phenyl)-amineHCID 11639307—
Edukt2-Bromo-1,4-bis(acetyloxymethyl)benzeneHCID 18504280—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelWaterHCID 962—
Produkt2-(4-Diphenylaminophenyl)-1,4-bis(acetyloxymethyl)benzeneHCID 1850427975,2%

Reaktionsschritte

4-Diphenylamino-1-(4,4,5,5-tetramethyl-1,3,2-Dioxaborolan-2-yl)benzene (6.09 g) (prepared by successive reaction of 4-bromo-triphenylamine with butyllithium and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane), 2-bromo-1,4-bis(acetyloxymethyl)benzene (4.9 g), tetrakis(triphenylphosphine)-palladium(0) (0.15 g), toluene (15 mL), and an aqueous solution of sodium carbonate (2M, 25 mL) were mixed under argon. The resulting mixture was stirred at reflux for 2 days, cooled, and poured into water. The aqueous mixture was then extracted with ether. The etheral solution was washed with dilute HCl, brine, dried with magnesium sulfate, and evaporated. The residue was recrystallized in methanol to yield 5.70 g of 2-(4-diphenylamino-phenyl)-1,4-bis(acetyloxymethyl)benzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06593687B1
Quelldatensatzuspto-grants-2003_07
ORD IDord-b03acb7ee9654658983403b6ea40505a
Quellennotizuspto-grants-2003_07