HRID484387

反应详情

EQUATION

反应方程式

HRID 484387 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 1,4,4,5,5-pentamethylimidazolidin-2-one (14 mg; 0.091 mmol) in dry tetrahydrofuran (0.2 ml), a 1.57 N solution of n-butyl lithium in hexane (0.06 ml; 0.1 mmol) was added at 0° C. After 5 minutes, a solution of 2-bromopropionyl bromide (24 mg; 0.11 mmol) in dry tetrahydrofuran (0.1 ml) was added thereto at the same temperature and followed by stirring for 10 minutes. A phosphate buffer (pH 7.0) was added to decompose the excess reaction agent. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were successively washed with a 5% aqueous solution of sodium bicarbonate and brine and dried over anhydrous magnesium sulfate. After removal of the solvent under reduced pressure, the residue was purified by preparative thin layer chromatography (benzene:ethyl acetate=5:1) to give 3-(2'-bromopropionyl)-1,4,4,5,5-pentamethylimidazolidin-2-one.

WORKUP

后处理

  1. extractionThe aqueous layer was extracted with ethyl acetate
  2. washthe combined organic layers were successively washed with a 5% aqueous solution of sodium bicarbonate and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customAfter removal of the solvent under reduced pressure
  5. customthe residue was purified by preparative thin layer chromatography (benzene:ethyl acetate=5:1)