HRID1242365
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
0.311 g (1.046 mmol) of the above prepared [2-methoxymethyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanol was dissolved in 4 ml of CH2Cl2 and treated at 0C. with 0.15 ml (2 eq.) of SOCl2. The reaction mixture was kept at 0° C. for 5 Min. and at ambient temperature for 60 Min. Pouring onto crashed ice/NaHCO3, twofold extraction with AcOEt, washing with water and brine, drying over magnesium sulfate, and evaporation of the solvents produced 0.330 g of pure title compound as colorless oil.
WORKUP
后处理
- customwas kept at 0° C. for 5 Min
- customat ambient temperature
- additionPouring
- extractionice/NaHCO3, twofold extraction with AcOEt
- washwashing with water and brine
- dry with materialdrying over magnesium sulfate, and evaporation of the solvents