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
2 g of 9H-Xanthene-9-carboxylic acid (0.0088 mol) were dissolved in 30 ml of CHCl3 (ethanol free). The solution was cooled at 0° C. and 1.08 ml (0.0123 mol) of oxalyl chloride and a drop of DMF was added. The mixture was stirred and allowed to warm to room temperature. After an hour at this temperature the solvents were evaporated and the residue was dissolved in CHCl3 and evaporated again. This procedure was repeated two times. The solid obtained (2.19 g) was dissolved in 20 ml of CHCl3 and added to a solution of 0.975 g (0.0097 mol) of (3R)-1-methylpyrrolidin-3-ol (Intermediate I-19) in 15 ml of CHCl3 cooled at 0–5° C. The reaction mixture was allowed to warm to room temperature and stirred overnight. The solvent was evaporated and the residue was dissolved in toluene and extracted with HCl 2N. The aqueous layer was basified with K2CO3 and extracted with CHCl3. The organic layer was washed with brine, dried over Na2SO4 and evaporated to dryness to yield 2.53 g (93%) of the title product as an oil.
WORKUP
后处理
- temperatureto warm to room temperature
- customAfter an hour at this temperature the solvents were evaporated
- dissolutionthe residue was dissolved in CHCl3
- customevaporated again
- customThe solid obtained (2.19 g)
- temperaturecooled at 0–5° C
- temperatureto warm to room temperature
- stirringstirred overnight
- customThe solvent was evaporated
- dissolutionthe residue was dissolved in toluene
- extractionextracted with HCl 2N
- extractionextracted with CHCl3
- washThe organic layer was washed with brine
- dry with materialdried over Na2SO4
- customevaporated to dryness