HRID483178

反应详情

EQUATION

反应方程式

HRID 483178 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

In 100 ml of ethanol, 1.66 g of ethyl p-chlorobenzate, 0.5 g of sodium ethylate and 2.09 g of 2-amino-3-(2-quinolon-3-yl)propionic acid were added and the whole mixture was placed in an autoclave. The reaction was carried out under 110 atmospheric pressure at 140°-150° C. for 6 hours. After completion of the reaction, the reaction mixture was cooled and concentrated under a reduced pressure. The residue was dissolved in 200 ml of chloroform, washed with 1%-potassium carbonate aqueous solution, a diluted hydrochloric acid and water in this order, then the chloroform layer was dried with sodium sulfate. The solvent was removed by distillation, the residue was recrystallized from ethanol-water to obtain 300 mg of 2-(4-chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid in the form of white powdery product.

WORKUP

后处理

  1. customAfter completion of the reaction
  2. temperaturethe reaction mixture was cooled
  3. concentrationconcentrated under a reduced pressure
  4. dissolutionThe residue was dissolved in 200 ml of chloroform
  5. washwashed with 1%-potassium carbonate aqueous solution
  6. dry with materiala diluted hydrochloric acid and water in this order, then the chloroform layer was dried with sodium sulfate
  7. customThe solvent was removed by distillation
  8. customthe residue was recrystallized from ethanol-water