HRID2232425

反应详情

EQUATION

反应方程式

HRID 2232425 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

In 60 ml of formic acid is dissolved 3.2 g of 7β-amino-3-(3-oxobutyryloxymethyl)-3-cephem-4-carboxylic acid and the solution is cooled to 0°-5° C. With stirring, 20 ml of acetic anhydride is added dropwise to the solution during 30 minutes. The mixture is stirred at the same temperature for 30 minutes and then at room temperature for 1 hour. The solvent is evaporated off under reduced pressure and the residue is dissolved in methyl ethyl ketone. The solution is washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then evaporated off under reduced pressure and a diisopropylether-hexane mixture is added to the residue to bring about solidification. The solid is then collected by filtration to give 3.1 g of the above-identified compound as a light-yellow powder. IR spectrum νmaxKBr cm-1 : 3380, 1780, 1720, 1660, 1625, 1510.

WORKUP

后处理

  1. temperaturethe solution is cooled to 0°-5° C
  2. stirringThe mixture is stirred at the same temperature for 30 minutes
  3. customThe solvent is evaporated off under reduced pressure
  4. dissolutionthe residue is dissolved in methyl ethyl ketone
  5. washThe solution is washed with water and saturated aqueous sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent is then evaporated off under reduced pressure
  8. additiona diisopropylether-hexane mixture is added to the residue
  9. filtrationThe solid is then collected by filtration