HRID1393364

反应详情

EQUATION

反应方程式

HRID 1393364 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

n-Butyl lithium (1.5 M n-hexane solution; 6.06 ml, 9.09 mmol) was added dropwise to a solution of 5-bromo-2-dimethylaminopyrimidine (1.75 g, 8.66 mmol) in tetrahydrofuran (18 ml) at −78° C. under argon atmosphere in 15 min. The mixture was stirred at the same temperature for 2 hrs. and then tri-n-butyltin chloride (2.5 ml) was added dropwise thereto. The mixture was stirred at the same temperature for 0.5 hrs. and then at room temperature for 1 hr. To the reaction mixture were added 10% aqueous potassium fluoride (50 ml) and ethyl acetate (50 ml) in turn and the mixture was stirred at room temperature for 0.5 hrs. The organic layer was separated and washed with water and brine in turn and dried. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography on amine silica gel (Chromatolex (trademark) NH) (n-hexane) to give 5-tri-n-butylstannyl-2-dimethylaminopyrimidine (2.65 g, 74%) as a colorless oil.

WORKUP

后处理

  1. stirringThe mixture was stirred at the same temperature for 0.5 hrs
  2. waitand then at room temperature for 1 hr
  3. stirringthe mixture was stirred at room temperature for 0.5 hrs
  4. customThe organic layer was separated
  5. washwashed with water and brine in turn
  6. customdried
  7. distillationThe solvent was distilled off under reduced pressure
  8. customthe residue was purified by column chromatography on amine silica gel (Chromatolex (trademark) NH) (n-hexane)