HRID476303

反应详情

EQUATION

反应方程式

HRID 476303 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

2-Bromo-N-[1-dimethylaminometh-(E)-ylidene]benzenesulfonamide (5.36 g, 18.4 mmol), 4-methylphenylboronic acid (5.0 g, 36.8 mmol), potassium carbonate (5.1 g, 36.8 mmol), water (19.7 mL, 1090 mmol), EtOH (49.2 mL, 842 mmol) and toluene (98.3 mL, 923 mmol) were combined and the mixture was stirred under nitrogen. Tetrakis(triphenylphosphine)palladium(0) (1.4 g, 1.2 mmol) was then added. The mixture was heated at 60° C. for about 2 hours, then heated at 70° C. for 30 minutes. The mixture was then cooled to room temperature and water (100 mL) and EtOAc (100 mL) were added. The mixture was washed with saturated aqueous NaCl, extracted with EtOAc, dried over MgSO4, filtered through Celite® and concentrated to yield the crude product as a red solid (8.6 g). The solid material was triturated with 1:1 EtOAc:hexanes, filtered, and rinsed with hexanes to yield the crude product as a reddish-brown solid (6.2 g). The solid material was again triturated with EtOAc, filtered, and rinsed with EtOAc to yield 4′-methybiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide as a light brown solid (4.6 g; 96.2% purity).

WORKUP

后处理

  1. temperatureheated at 70° C. for 30 minutes
  2. temperatureThe mixture was then cooled to room temperature
  3. washThe mixture was washed with saturated aqueous NaCl
  4. extractionextracted with EtOAc
  5. dry with materialdried over MgSO4
  6. filtrationfiltered through Celite®
  7. concentrationconcentrated
  8. customto yield the crude product as a red solid (8.6 g)
  9. customThe solid material was triturated with 1:1 EtOAc
  10. filtrationhexanes, filtered
  11. washrinsed with hexanes
  12. customto yield the crude product as a reddish-brown solid (6.2 g)
  13. customThe solid material was again triturated with EtOAc
  14. filtrationfiltered
  15. washrinsed with EtOAc