HRID2234082

反应详情

EQUATION

反应方程式

HRID 2234082 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of 0.93 g 2,2,6,6-tetramethylpiperidine in 30 ml THF is added 4.13 ml (15% solution in toluene) n-butyllithium at −30° C. After being stirred at 0° C. for 30 min, the reaction mixture is cooled to −78° C. and a solution of 1.12 g 3-methoxy-6-pyridin-4-yl-pyridazine in 30 ml THF is added and stirred at −78° C. for 30 min. At this temperature 3.17 g acetaldehyde are added and stirred for another 2 h. The reaction is quenched by the addition of 24 ml MeOH/THF 1:1 and warmed to ambient temperature. Than 30 ml saturated aq. NaHCO3 are added and extracted with CH2Cl2. The combined organic layers are washed with water, dried over MgSO4 and concentrated in vacuo. The residue is purified by flash chromatography (ethyl acetate 100%) to give 0.91 g (66%) of the desired product as a beige solid.

WORKUP

后处理

  1. temperaturethe reaction mixture is cooled to −78° C.
  2. stirringstirred at −78° C. for 30 min
  3. stirringstirred for another 2 h
  4. customThe reaction is quenched by the addition of 24 ml MeOH/THF 1:1
  5. temperaturewarmed to ambient temperature
  6. additionThan 30 ml saturated aq. NaHCO3 are added
  7. extractionextracted with CH2Cl2
  8. washThe combined organic layers are washed with water
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. customThe residue is purified by flash chromatography (ethyl acetate 100%)