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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67788Erstellt: 24. Oktober 2026

Benzene → [1,1'-Biphenyl]-4,4'-diamine, N4,N4'-bis(3-methylphenyl)-N4,N4'-diphenyl-

https://huagongshe.com/de/reaction/67788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktDimethyl SulfoxideHCID 679—
EduktPotassium CarbonateHCID 11430—
Edukt3-IodotolueneHCID 12268—
EduktN,N'-DiphenylbenzidineHCID 68280—
KatalysatorCopperHCID 23978—
Produkt[1,1'-Biphenyl]-4,4'-diamine, N4,N4'-bis(3-methylphenyl)-N4,N4'-diphenyl-HCID 103315—

Reaktionsschritte

In a 5000 milliliter, round bottom, 3 necked flask fitted with a mechanical stirrer and blanketed with argon, is placed 336 grams (1 mole) of N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine, 550 grams (2.5 moles) of m-iodotoluene, 550 grams (4 moles) potassium carbonate (anhydrous) and 50 grams of copper bronze catalyst and 1500 ml dimethylsulfoxide (anhydrous). The heterogeneous mixture is refluxed for 6 days. The mixture is allowed to cool. 2000 ml of benzene is added. The dark slurry is then filtered. The filtrate is extracted 4 times with water. Then the filtrate is dried with magnesium sulfate and filtered. The benzene is taken off under reduced pressure. The black product is column chromatographed using Woelm neutral alumina. Colorless crystals of the product are obtained by recrystallizing the product from n-octane. The melting point is 167°-169° C. The yield is 360 grams (65%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04346158
Quelldatensatzuspto-grants-1982_08
ORD IDord-86a6dc0eacb141b18be93852b04c1774
Quellennotizuspto-grants-1982_08