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
To a solution of methyl 4-(2-t-butyldimethylsiloxyethyl)cinnamate (1.53 g) in ethanol (25 ml) was added a 10% palladium on activated carbon (0.15 g), and the mixture was stirred at room temperature for 2 hours under an atmosphere of hydrogen. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. To a solution of the residue in tetrahydrofuran (35 ml) was added lithium bis(trimethylsilyl)amide (1.0 mol/l solution in tetrahydrofuran, 3.9 ml) at -78° C., and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added a solution of iodomethane (0.533 g) in tetrahydrofuran (2 ml), and the mixture was stirred at room temperature for 1 hour. To the reaction mixture was added water, and the mixture was extracted with diethyl ether. The extract was washed with water, and dried over anhydrous MgSO4. The solvent was removed under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on a silica gel column using a mixture of n-hexane and methylene chloride (3:1) as eluent to give 1-(2-t-butyldimethylsiloxyethyl)-4-(2-methoxycarbonylpropyl)benzene (0.724 g) as a colorless oily liquid.
WORKUP
后处理
- customThe catalyst was removed by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- additionTo a solution of the residue in tetrahydrofuran (35 ml) was added lithium bis(trimethylsilyl)amide (1.0 mol/l solution in tetrahydrofuran, 3.9 ml) at -78° C.
- stirringthe mixture was stirred at the same temperature for 30 minutes
- additionTo the reaction mixture was added a solution of iodomethane (0.533 g) in tetrahydrofuran (2 ml)
- stirringthe mixture was stirred at room temperature for 1 hour
- additionTo the reaction mixture was added water
- extractionthe mixture was extracted with diethyl ether
- washThe extract was washed with water
- dry with materialdried over anhydrous MgSO4
- customThe solvent was removed under reduced pressure
- customthe residue was purified by medium pressure liquid column chromatography on a silica gel column
- additiona mixture of n-hexane and methylene chloride (3:1) as eluent