Reaktion #73733

ord-da2289bbb0d444e6a1e174ec6f92aef7

Reaktionsgleichung

COc1ccccc1B(O)O
2-methoxyphenylboronic acid
Brc1cccc(Br)c1
3,5-dibromobenzene
O=C([O-])O.[Na+]
sodium bicarbonate
COc1ccccc1-c1cccc(Br)c1
21
Ausbeute 190.7%
COc1ccccc1-c1cccc(Br)c1
3′-Bromo-2-methoxybiphenyl
Ausbeute 190.7%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux under nitrogen
  2. 2
    TemperaturAfter cooling
  3. 3
    Sonstigethe reaction mixture was partitioned between ethyl acetate (600 mL) and water (300 mL)
  4. 4
    WaschenThe organic phase was washed with water (2×300 mL)
  5. 5
    Trocknendried over sodium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    SonstigeThe solvent was removed in vacuo
  8. 8
    Sonstigethe crude product was purified by chromatography on silica (150 g) with heptane (6 L)

Vorschrift

A mixture of 2-methoxyphenylboronic acid (4.3 g, 28.3 mmol), 3,5-dibromobenzene (20 g, 85.5 mmol, 3 equiv.) and bis(triphenylphosphine)palladium(II) dichloride (100 mg) in ethyleneglycol dimethylether (25 mL) and a solution of sodium bicarbonate (8.2 g, 0.098 mol) in water (140 mL) were kept at reflux under nitrogen with good stirring overnight. After cooling, the reaction mixture was partitioned between ethyl acetate (600 mL) and water (300 mL). The organic phase was washed with water (2×300 mL), dried over sodium sulfate and filtered. The solvent was removed in vacuo and the crude product was purified by chromatography on silica (150 g) with heptane (6 L) to afford pure 21 (14.2 g, 58%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541522B2uspto-grants-2013_09