HRID413565
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
(±)-7-(4-fluorophenoxy)-6-(2-methoxyethoxymethoxy)heptan-1-al 45 (2 g, 6.1 mmol) and 2 ml of trifluoroacetic acid are added to 10 ml of chloroform. The reaction mixture is stirred for 24 hours and then is neutralized with 1% aqueous NaOH. The organic layer is washed with water, brine, dried (Na2SO4), concentrated. The crude trifluoroacetyl-aldehyde 46 is then dissolved in MeOH:H2O (1:1) and solid K2CO3 is added to maintain pH 8. The reaction is complete is approximately 15 minutes, as monitored by TLC (ethyl acetate:hexane 3:7). Methanol is removed in vacuo and remaining solution is extracted with ethyl acetate to give (±)-7-(4-fluorophenoxy)-6-(hydroxy)-heptan-al 47 (1.2 g, 82%).
WORKUP
后处理
- washThe organic layer is washed with water, brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- dissolutionThe crude trifluoroacetyl-aldehyde 46 is then dissolved in MeOH:H2O (1:1)
- additionsolid K2CO3 is added
- temperatureto maintain pH 8
- waitThe reaction is complete is approximately 15 minutes
- customMethanol is removed in vacuo
- extractionis extracted with ethyl acetate