HRID1417032

反应详情

EQUATION

反应方程式

HRID 1417032 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

A mixture of 12-(3-bromo-1-propylidene)-12H-dibenzo[d,g][1,3]dioxocine (4.0 g, 12 mmol, prepared as described in example 1), 4-piperidinecarboxylic acid ethyl ester (1.9 g, 12 mmol), anhydrous potassium carbonate (5.0 g) and sodium iodide (0.2 g) in N,N-dimethylformamide (40 ml) was heated at 60-70° C. for 5 h. After cooling, the inorganic salts were filtered off and washed with benzene (40 ml), and the filtrate was diluted with additional benzene (120 ml). The benzene solution was washed with water (3×50 ml), dried over MgSO4 and evaporated in vacuo. The oily residue (4.8 g) was purified by chromatography on silica gel using a mixture of benzene and ethyl acetate as eluent to give 1-(3-(12H-dibenzo[d,g][1,3]dioxocin-12-ylidene)-1-propyl)-4-piperidinecarboxylic acid ethyl ester as an oil (2.3 g, 47%).

WORKUP

后处理

  1. temperatureAfter cooling
  2. filtrationthe inorganic salts were filtered off
  3. washwashed with benzene (40 ml)
  4. additionthe filtrate was diluted with additional benzene (120 ml)
  5. washThe benzene solution was washed with water (3×50 ml)
  6. dry with materialdried over MgSO4
  7. customevaporated in vacuo
  8. customThe oily residue (4.8 g) was purified by chromatography on silica gel using
  9. additiona mixture of benzene and ethyl acetate as eluent