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
10.57 g of 1-(2,4-dimethoxyphenyl)ethanone are dissolved in 100 ml of ether and 50 ml of THF under nitrogen. 55 ml of 1.6M methyllithium in ether are added at −50° C. and the mixture is left stirring for 2 hours between −60° C. and −40° C. and then for 30 minutes between −40° C. and 0° C. and for 3 hours at RT. It is cooled to 0° C. and 70 ml of 2N HCl are added. After separation of the phases by settling, the aqueous phase is extracted with ether and the organic phase is then dried over Na2SO4. This solution is concentrated and the residue is then taken up in 150 ml of THF and 75 ml of 2N HCl are added. After stirring for 4 hours at RT, 100 ml of water are added and this mixture is then extracted with ether. The organic phase is washed with Na2CO3, with water and then dried over Na2SO4 and concentrated. The residue is chromatographed on silica, eluting with a DCM/pentane mixture (70/30 and then 60/40). 5 g of the expected compound are obtained in the form of an oil.
WORKUP
后处理
- waitthe mixture is left
- waitfor 30 minutes between −40° C. and 0° C.
- waitfor 3 hours at RT
- customAfter separation of the phases
- extractionthe aqueous phase is extracted with ether
- dry with materialthe organic phase is then dried over Na2SO4
- concentrationThis solution is concentrated
- addition75 ml of 2N HCl are added
- stirringAfter stirring for 4 hours at RT
- addition100 ml of water are added
- extractionthis mixture is then extracted with ether
- washThe organic phase is washed with Na2CO3, with water
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe residue is chromatographed on silica
- washeluting with a DCM/pentane mixture (70/30