HRID1709370

反应详情

EQUATION

反应方程式

HRID 1709370 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

6.1 g (25 mmol) of t-butyl 2-(2-amino-4-thiazolyl)-2-(Z)-hydroxyimino-acetate are dispersed in 250 ml of dry acetonitrile. 13.7 g (50 mmol) of p-nitrobenzyl bromoacetate and 12.9 ml (75 mmol) of N-ethyldiisopropylamine are now added thereto at room temperature while stirring. 7.5 g (50 mmol) of sodium iodide are added thereto 5 minutes later. The mixture is stirred at room temperature for 3.5 hours in an argon atmosphere. The solvent is subsequently removed by evaporation and the residue is diluted with 500 ml of ethyl acetate. The solution obtained is washed four times with a total of 2 l of water. The aqueous phase is extracted with 300 ml of ethyl acetate and the combined ethyl acetate solutions are dried over sodium sulphate and evaporated to dryness. After crystallization from ethyl acetate/hexane, there are obtained 8.2 g (75%) of t-butyl 2-(2-amino-4-thiazolyl)-2-[[(p-nitrobenzyloxycarbonyl)methoxy]imino]-acetate of melting point 146.8° C. (decomposition).

WORKUP

后处理

  1. custom5 minutes
  2. stirringThe mixture is stirred at room temperature for 3.5 hours in an argon atmosphere
  3. customThe solvent is subsequently removed by evaporation
  4. additionthe residue is diluted with 500 ml of ethyl acetate
  5. customThe solution obtained
  6. washis washed four times with a total of 2 l of water
  7. extractionThe aqueous phase is extracted with 300 ml of ethyl acetate
  8. dry with materialthe combined ethyl acetate solutions are dried over sodium sulphate
  9. customevaporated to dryness
  10. customAfter crystallization from ethyl acetate/hexane, there