HRID512180
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
PROCEDURE
实验过程
A solution of 2-(2-methylpyrimidin-5-yl)acetonitrile (4 g, 0.03 amol) and methyl acrylate (5.69 g, 0.066 mol) in THF (60 mL) was added t-BuOK (93 mL, 0.093 mol, 1M in THF) and stirred at room temperature for 4 h. The reaction mixture was quenched by sat. NH4Cl and extracted with EtOAc (3×150 mL). The organic layer was dried over Na2SO4 and concentracted to give methyl 5-cyano-2-hydroxy-5-(2-methylpyrimidin-5-yl)cyclohex-1-enecarboxylate (5.5 g), which was used for the next step directly.
WORKUP
后处理
- customThe reaction mixture was quenched by sat. NH4Cl
- extractionextracted with EtOAc (3×150 mL)
- dry with materialThe organic layer was dried over Na2SO4