HRID382462

反应详情

EQUATION

反应方程式

HRID 382462 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
107.5 °C

PROCEDURE

实验过程

Under a nitrogen atmosphere, a mixture of N-methyl-N-(3-buten-1-yl)benzamide (2.15 g, 11.36 mmol), 3-iodoaniline (2.49 g, 11.36 mmol, Aldrich Chemical Company), palladium(II) acetate (25.5 mg, 0.11 mmol), and triethylamine (2.30 g, 22.70 mmol) was stirred and heated under reflux at 105-110° C. (oil bath temperature) for 52 h. The dark-brown solution was allowed to cool to ambient temperature and was diluted with water (20 mL) and CHCl3 (40 mL). The water layer was separated and extracted with CHCl3 (2×10 mL). The combined CHCl3 extracts were washed with saturated NaCl solution (10 mL), dried (CHCl3), filtered, and concentrated by rotary evaporation. Further drying under high vacuum (0.3 mm Hg) for 15 h produced a viscous, brown oil (3.59 g). The crude material was purified by column chromatography on silica gel (155.5 g, 4.0 cm i.d.×60.5 cm column) eluting with EtOAc (25→67%, v/v) in CHCl3. Fractions containing the product (Rf 0.34 in EtOAc-CHCl3, 1:1, v/v) were combined, concentrated by rotary evaporation, and vacuum dried at 45° C. for 15 h to give 1.60 g (50.2%) of an amber oil.

WORKUP

后处理

  1. temperatureheated
  2. temperatureto cool to ambient temperature
  3. customThe water layer was separated
  4. extractionextracted with CHCl3 (2×10 mL)
  5. washThe combined CHCl3 extracts were washed with saturated NaCl solution (10 mL)
  6. dry with materialdried (CHCl3)
  7. filtrationfiltered
  8. concentrationconcentrated by rotary evaporation
  9. customFurther drying under high vacuum (0.3 mm Hg) for 15 h