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
- -78 °C
PROCEDURE
实验过程
Titanocene dichloride (0.28 g, 1.1 mmol) was dissolved in (15 mL) of tetrahydrofuran in a nitrogen atmosphere, and the reaction mixture was cooled to -78° C., and 2.4 mL of a 1.6M solution of n-butyl lithium in hexane was added. The reaction mixture was stirred for 15 min and then 4.5 mL diphenylsilane (24 mmol) was added. After warming the reaction mixture to room temperature, 1.8 g of N-benzylpyrrolidinone (11 mmol) was added to the black solution, which began bubbling and became warm (i.e., about 30° C.) after 1-2 min. The reaction mixture was stirred overnight at room temperature and then heated to 55° C. for 1 hour. The solution was then poured into 50 mL of ethyl ether and extracted with 1 M HCl (3×50 mL). The aqueous layer was washed with ether (2×25 mL) and then neutralized with a 5 M NaOH solution so that the aqueous layer was basic to pH paper. The product was extracted into ether (3×50 mL) and the emulsion that formed was also extracted with ether (50 mL). The combined ether extracts were dried over MgSO4, filtered, and concentrated in vacuo. N-benzylpyrrolidine was isolated as a yellow oil (1.58 g of 95% pure material, 84% yield).
WORKUP
后处理
- temperatureAfter warming the reaction mixture to room temperature
- custombegan bubbling
- temperaturebecame warm (i.e., about 30° C.) after 1-2 min
- stirringThe reaction mixture was stirred overnight at room temperature
- temperatureheated to 55° C. for 1 hour
- additionThe solution was then poured into 50 mL of ethyl ether
- extractionextracted with 1 M HCl (3×50 mL)
- washThe aqueous layer was washed with ether (2×25 mL)
- extractionThe product was extracted into ether (3×50 mL)
- customthe emulsion that formed
- extractionwas also extracted with ether (50 mL)
- dry with materialThe combined ether extracts were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo