反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- temperaturethe reaction mixture is cooled to −78° C.
- stirringstirred at −78° C. for 30 min
- stirringstirred for another 2 h
- customThe reaction is quenched by the addition of 24 ml MeOH/THF 1:1
- temperaturewarmed to ambient temperature
- additionThan 30 ml saturated aq. NaHCO3 are added
- extractionextracted with CH2Cl2
- washThe combined organic layers are washed with water
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customThe residue is purified by flash chromatography (ethyl acetate 100%)