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

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).

1. temperatureThe reaction mixture is cooled to between −5° C. and 0° C.
2. temperaturethe reaction mixture is maintained at between −5 and 0° C. for 30-40 minutes
3. stirringstirred at 50° C. for 10-15 minutes
4. temperatureThe reaction mixture is cooled to room temperature
5. additionpoured into ice-cold water
6. extractionextracted with ethyl acetate (3×300 ml)
7. washThe organic extracts are washed with water
8. dry with materialdried over anhydrous sodium sulfate
9. concentrationconcentrated under reduced pressure
10. customThe residue is purified by column chromatography on silica gel

ORD-Eintrag

ord-6896fc7a72664a77bf2fce93654990c1

Quelldatensatz

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08828908B2