HRID1517738

反应详情

EQUATION

反应方程式

HRID 1517738 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

Compound A (80.0 g, 311 mmol) and 3-fluoro-4-methylphenylboronic acid (52.7 g, 342 mmol) were suspended in isopropyl alcohol (260 mL, 3.5 mol). A solution of sodium carbonate (56.1 g, 529 mmol) in water (260 mL, 15 mol) was added and the mixture was degassed under nitrogen. Tetrakis(triphenylphosphine)palladium(0) (3.6 g, 3.1 mmol) was then added and the mixture was stirred at 90° C. for 17 hours. The mixture was concentrated under reduced pressure and suspended in water (200 mL). The aqueous phase was extracted with EtOAc (600 mL) and separated. The organic phase was washed with saturated aqueous NaCl and concentrated under reduced pressure. The recovered oil was purified by silica gel chromatography (4-6% 5×120 g column) to yield compound B as a clear oil (68.2 g).

WORKUP

后处理

  1. customthe mixture was degassed under nitrogen
  2. concentrationThe mixture was concentrated under reduced pressure
  3. extractionThe aqueous phase was extracted with EtOAc (600 mL)
  4. customseparated
  5. washThe organic phase was washed with saturated aqueous NaCl
  6. concentrationconcentrated under reduced pressure
  7. customThe recovered oil was purified by silica gel chromatography (4-6% 5×120 g column)