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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72295Erstellt: 24. Oktober 2026

Hydrogen Bromide → 4-Bromo-4'-chloro-3-methylbiphenyl

https://huagongshe.com/de/reaction/72295

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktAcetonitrileHCID 6342—
EduktButyl nitriteHCID 10996—
Edukt4'-Chloro-3-methylbiphen-4-ylamineHCID 23005188—
Katalysatorcopper(I) bromideHCID 24593—
Produkt4-Bromo-4'-chloro-3-methylbiphenylHCID 59450516—

Reaktionsschritte

4′-Chloro-3-methylbiphen-4-ylamine (16.5 g, 0.077 mol) is added to acetonitrile (140 ml) and stirred at room temperature until dissolution is complete. The reaction mixture is cooled to between −5° C. and 0° C., tent-butyl nitrite (90%, 12.4 ml, 0.093 mol) is added dropwise and the reaction mixture is maintained at between −5 and 0° C. for 30-40 minutes. The mixture is added slowly to the preheated (50° C.) suspension of copper (I) bromide (5.8 g, 0.04 mol) in hydrobromic acid (5.8 ml) and stirred at 50° C. for 10-15 minutes. The reaction mixture is cooled to room temperature, then poured into ice-cold water and extracted with ethyl acetate (3×300 ml). The organic extracts are washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to yield 4-bromo-4′-chloro-3-methylbiphenyl (11.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828908B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-6896fc7a72664a77bf2fce93654990c1
Quellennotizuspto-grants-2014_09