HRID50235

反应详情

EQUATION

反应方程式

HRID 50235 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 2.2 mL (15 mmol) of 1-methyl-4-methylaminopiperidine in 60 mL pyridine, 3.8 g (15 mmol) of 4-chloro-3-nitrobenzenesulfonic acid chloride were added, in batches, whilst cooling with ice. The mixture was then stirred for two hours with cooling, then evaporated to dryness, the residue was mixed with about 50 mL of water and made alkaline with concentrated ammonia whilst stirring vigorously. The crude product precipitated was suction filtered and purified by column chromatography (250 g silica gel, eluant: dichloromethane with 1.5% ethanol). Yield: 1.6 g (31% of theory), C13H18ClN3O4S (347.8); Rf value: 0.19 (silica gel; dichloromethane/ethanol=19:1).

WORKUP

后处理

  1. temperaturewhilst cooling with ice
  2. temperaturewith cooling
  3. customevaporated to dryness
  4. additionthe residue was mixed with about 50 mL of water
  5. stirringwhilst stirring vigorously
  6. customThe crude product precipitated
  7. filtrationfiltered
  8. custompurified by column chromatography (250 g silica gel, eluant: dichloromethane with 1.5% ethanol)