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
PROCEDURE
实验过程
To a 500-mL, three-necked, round-bottomed flask equipped with a magnetic stirring bar, a thermometer, and a condenser was charged tetrahydrofuran (163 mL), potassium tert-butoxide (6.6 g, 95% pure) and trimethylsulfoxonium iodide (13.0 g). The mixture was heated to reflux and stirred for 3 hours. A solution of benzyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate (10.0 g) in tetrahydrofuran (37 mL) was added in one portion. The reaction mixture was refluxed for another 2 hours. The mixture was cooled to room temperature and diluted with toluene (100 mL) and water. The water layer was separated and extracted with toluene (2×50 mL). The combined organic layers were washed with water (3×40 mL) and concentrated under vacuum to provide the title compound.
WORKUP
后处理
- customTo a 500-mL, three-necked, round-bottomed flask equipped with a magnetic stirring bar
- temperatureThe mixture was heated
- temperatureto reflux
- temperatureThe reaction mixture was refluxed for another 2 hours
- customThe water layer was separated
- extractionextracted with toluene (2×50 mL)
- washThe combined organic layers were washed with water (3×40 mL)
- concentrationconcentrated under vacuum