HRID2167163

反应详情

EQUATION

反应方程式

HRID 2167163 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

To an oven dried 50 mL pressure vessel equipped with magnetic stirring bar was added 6-chloromethyl-2,2′-bipyridine (BPy-CH2Cl) (2.05 g, 10.00 mmol), di-tert-butyl phosphine (1.75 g, 12.00 mmol), and 30 mL MeOH in a nitrogen glove box. The flask was sealed and heated at 50° C. for 48 hrs with stirring outside the glove box. After cooling, it was reintroduced to the glove box, triethylamine (1.82 g, 18.00 mmol) was added and the reaction mixture was stirred at room temperature for 1 hr. The solvents were removed under reduced pressure to obtain a white solid. The residue was washed with ether (3×20 mL) and the ether filtered and was removed under reduced pressure to yield a white solid. It was recrystallized from MeOH at ca. −30° C. to yield 2.67 g (85%) of 6-di-tert-butylphosphinomethyl-2,2′-bipyridine (BPy-tPNN).

WORKUP

后处理

  1. customTo an oven dried 50 mL pressure vessel
  2. customequipped with magnetic stirring bar
  3. customThe flask was sealed
  4. temperatureAfter cooling
  5. additionwas added
  6. stirringthe reaction mixture was stirred at room temperature for 1 hr
  7. customThe solvents were removed under reduced pressure
  8. customto obtain a white solid
  9. washThe residue was washed with ether (3×20 mL)
  10. filtrationthe ether filtered
  11. customwas removed under reduced pressure
  12. customto yield a white solid
  13. customIt was recrystallized from MeOH at ca. −30° C.