HRID549932

反应详情

EQUATION

反应方程式

HRID 549932 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Benzyl 4-{[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]methyl}piperazine-1-carboxylate (4.46 g) was stirred in a mixture of trifluoroacetic acid (20 ml) and dichloromethane (200 ml) for two hours at room temperature. The reaction mixture was concentrated in vacuo and the resulting oil separated between ethyl acetate (200 ml) and saturated aqueous sodium bicarbonate solution (500 ml). The ethyl acetate layer was separated, dried over magnesium sulphate, filtered then concentrated in vacuo to give the title compound (3.6 g).

WORKUP

后处理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customthe resulting oil separated between ethyl acetate (200 ml) and saturated aqueous sodium bicarbonate solution (500 ml)
  3. customThe ethyl acetate layer was separated
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. concentrationthen concentrated in vacuo