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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11746Erstellt: 24. Oktober 2026

Nitrobenzene → 4,4'-Dibromo-2-bis(4-methoxyphenyl)amino-1,1'-biphenyl

https://huagongshe.com/de/reaction/11746

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrobenzeneHCID 7416—
EduktPotassium CarbonateHCID 11430—
Edukt4-IodoanisoleHCID 69676—
Edukt5-Bromo-2-(4-bromophenyl)anilineHCID 4559420—
KatalysatorCopperHCID 23978—
LösungsmittelTolueneHCID 1140—
Produkt4,4'-Dibromo-2-bis(4-methoxyphenyl)amino-1,1'-biphenylHCID 21976314—

Reaktionsschritte

4,4′-Dibromo-2-amino-1,1′-biphenyl (16.35 g, 0.05 mol), 4-iodoanisole (28 g, 0.12 mol), potassium carbonate (−325 mesh fine powder, 16.6 g, 0.12 mole), copper dust (−150 mesh,1.0 g), and nitrobenzene (20 ml) were charged into a flask and stirred at gentle reflux for 15 hours. The dark reaction mixture was cooled to room temperature and extracted with 200 ml of toluene. The toluene solution was evaporated. The dark residue obtained was then mixed with 10 ml of toluene and chromatographed on a silica gel column using hexane and hexane/ethyl acetate (20:1) eluant. The portions containing the product were collected and evaporated. The residue was recrystallized twice from hexane/toluene (300 ml/60 ml) to yield 7.4 grams of off-white crystals of the desired monomer. 1H NMR (CDCl3): δ=6.8–7.5 (15H, multiple peaks); 3.78 (6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098297B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1b201015aa3a453fafae9c0c128bc49f
Quellennotizuspto-grants-2006_08