HRID2140

反应详情

EQUATION

反应方程式

HRID 2140 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-10 °C

PROCEDURE

实验过程

A solution of 2-(methanesulphonyloxy)methoxybenzene (0.822 g) in dichloromethane (15 ml) was stirred and cooled to -10° C. under a nitrogen atmosphere. A solution of chlorosulphonic acid (0.27 ml) in dichloromethane (5 ml) was then added dropwise over a period of 1 hour, maintaining the temperature below 0° C. The mixture was stirred for a further 4 hours, allowing the temperature to rise to 10° C. The mixture was evaporated to dryness in vacuo to yield an oil which was suspended in toluene (20 ml) with stirring under a nitrogen atmosphere. Oxalyl chloride (0.36 ml) was added dropwise, followed by the addition of DMF (5 drops). After stirring for 2 hours at room temperature, dichloromethane (15 ml) and oxalyl chloride (0.36 ml) were added and the reaction stirred overnight. The solvent was evaporated in vacuo and the residue was purified by column chromatography on silica, eluting with 60% ethyl acetate in hexane to furnish the title compound (0.99 g) as a white crystalline solid.

WORKUP

后处理

  1. temperaturemaintaining the temperature below 0° C
  2. customto rise to 10° C
  3. customThe mixture was evaporated to dryness in vacuo
  4. customto yield an oil which
  5. stirringwith stirring under a nitrogen atmosphere
  6. stirringAfter stirring for 2 hours at room temperature
  7. stirringthe reaction stirred overnight
  8. customThe solvent was evaporated in vacuo
  9. customthe residue was purified by column chromatography on silica
  10. washeluting with 60% ethyl acetate in hexane