Реакция #1605815

ord-44fedd1f22a34adb8e981105e0614b93

Уравнение реакции

COc1ccc(Br)c([N+](=O)[O-])c1
1-Bromo-4-methoxy-2-nitrobenzene
OB(O)Oc1ccccc1
phenyl boric acid
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
COc1ccc(-c2ccccc2)c([N+](=O)[O-])c1
4-methoxy-2-nitro-1-phenylbenzene
Выход 81.1%

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеpurified water (12 mL)
  2. 2
    ФильтрацияThe reaction solution was filtered through celite, alumina, and Florisil
  3. 3
    Экстракцияextracted with ethyl acetate
  4. 4
    ПромывкаThe organic layer was washed with a saturated aqueous solution of sodium chloride
  5. 5
    Сушкаdried over anhydrous magnesium sulfate
  6. 6
    Концентрированиеconcentrated under reduced pressure
  7. 7
    ДругоеThe residue was purified by flash column chromatography

Методика

1-Bromo-4-methoxy-2-nitrobenzene (2.32 g, 10 mmol) was dissolved in 1,4-dioxane (30 mL) and, thereto, were added phenyl boric acid (2.44 g, 20 mmol), cesium carbonate (26 g, 80 mmol), 1,1-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane complex (0.82 g, 1 mmol), and purified water (12 mL). The reaction mixture was stirred under a nitrogen flow at 80° C. for 18 hours. The reaction solution was filtered through celite, alumina, and Florisil, and, thereafter, extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography to obtain 4-methoxy-2-nitro-1-phenylbenzene (1.86 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09072734B2uspto-grants-2015_07