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
In a 1 L round bottom flask, 6-(3-chloro-propoxy)-3,4-dihydro-2H-naphthalen-1-one (10.0 g, 41.9 mmol), benzenesulfonate (R)-2-methyl-pyrrolidinium (13.15 g, 84.0 mmol), potassium carbonate (23.15 g, 168 mmol), and potassium iodide (100 mg, 0.6 mmol) in acetonitrile (600 mL) was heated to reflux 14 h. The reaction was cooled and the solvent concentrated under vacuum. The slurry was partitioned between methylene chloride and water, then washed with water three times. The organics were extracted three times with 3% citric acid solution. The combined aqueous layers were basified with sat. NaHCO3 sol. and extracted with methylene chloride, then dried over MgSO4. Ethereal HCl was added and the solvents reduced under vacuum. Crystallization from MeOH/Et2O produced 8.75 g (65%). Mp 183-185° C. MS m/z=288 (M+H).
WORKUP
后处理
- temperatureto reflux 14 h
- temperatureThe reaction was cooled
- concentrationthe solvent concentrated under vacuum
- customThe slurry was partitioned between methylene chloride and water
- washwashed with water three times
- extractionThe organics were extracted three times with 3% citric acid solution
- extractionextracted with methylene chloride
- dry with materialdried over MgSO4
- additionEthereal HCl was added
- customCrystallization from MeOH/Et2O
- customproduced 8.75 g (65%)