HRID27968

反应详情

EQUATION

反应方程式

HRID 27968 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

10 g of the syn isomer of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid containing 7.2% of ethanol were added to a solution of 2 g of sodium acetate in 7.5 ml of water and 20 ml of absolute ethanol and the mixture was stirred for 15 minutes, was treated with 1.5 g of activated carbon and was filtered. The filter was washed twice with 5 ml of a 9-1 ethanol-water mixture and the filtrate was added dropwise over 50 minutes with stirring at room temperature to 80 ml of ethanol which caused precipitation of the sodium salt. The mixture was stirred for 2 hours at 0° C. and was vacuum filtered. The crystals were washed with ethanol and dried under reduced pressure to obtain 8.45 g of the crystalline D form of the syn isomer of sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme- 4-carboxylate containing 5.7% of water.

WORKUP

后处理

  1. additionwas treated with 1.5 g of activated carbon
  2. filtrationwas filtered
  3. washThe filter was washed twice with 5 ml of a 9-1 ethanol-water mixture
  4. additionthe filtrate was added dropwise over 50 minutes
  5. stirringwith stirring at room temperature to 80 ml of ethanol which
  6. customprecipitation of the sodium salt
  7. stirringThe mixture was stirred for 2 hours at 0° C.
  8. filtrationfiltered
  9. washThe crystals were washed with ethanol
  10. customdried under reduced pressure