HRID1421239
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
First, (R)-5-acetoxy-1-iodohexane was prepared in the following manner. A solution of (R)-5-acetoxy-1-chlorohexane (4.80 g:26.89 mmol) was added to sodium iodide (5.39 g:36 mmol) in a round bottomed flask fitted with magnetic stirrer bar and a reflux condenser and refluxed for 12 hrs with stirring. Acetone was removed under reduced pressure, The crude product was partitioned between ethyl acetate (50 ml) and water layer (60 ml). The organic layer was washed with 10% sodium thiosulphate solution followed by water (20 l), dried over anhydrous Mg SO4 and concentrated under reduced pressure. Yield=7 g (96%)
WORKUP
后处理
- customfitted with magnetic stirrer bar and a reflux condenser
- temperaturerefluxed for 12 hrs
- customAcetone was removed under reduced pressure
- customThe crude product was partitioned between ethyl acetate (50 ml) and water layer (60 ml)
- washThe organic layer was washed with 10% sodium thiosulphate solution
- dry with materialdried over anhydrous Mg SO4
- concentrationconcentrated under reduced pressure