HRID44648

反应详情

EQUATION

反应方程式

HRID 44648 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

45 g (0.1 mol) of di-tert-butyl 1-(1-acetylpiperidin-4-yl)-2-benzoylhydrazine-1,2-dicarboxylate were dissolved in 1 L of tetrahydrofuran and a solution of 5.8 g (0.14 mol) of lithium hydroxide monohydrate in 1 L of water were added. The mixture was stirred at room temperature for 16 hours, the tetrahydrofuran removed in vacuo and the aqueous layer extracted several times with dichloromethane. The organic phase was dried over sodium sulfate and evaporated to dryness, giving 32 g (84% yield) of the title compound.

WORKUP

后处理

  1. customthe tetrahydrofuran removed in vacuo
  2. extractionthe aqueous layer extracted several times with dichloromethane
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customevaporated to dryness