HRID441569

反应详情

EQUATION

反应方程式

HRID 441569 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
62 °C

PROCEDURE

实验过程

To a stirring mixture of 1.5 grams (0.0047 mole) of 3,4,5-trichloro-N,N-dimethyl-2-(mercapto)benzenesulfonamide in 80 milliliters of methanol at 25° C., was added 0.39 grams of sodium methoxide. The mixture was stirred for 15 minutes and thereafter 1.0 gram (0.009 mole) of chloromethylthiocyanate was added thereto and the mixture stirred at room temperature for 3 hours. At the end of this time period, the reaction mixture was filtered to remove the solids which had precipitated. The filtrate further heated at 62° C. for 2 hours and after cooling, the solvent was reduced in volume by evaporation under reduced pressure. The solids were thereafter removed by filtration. Additional filtrations gave additional solids. The recovered solids were combined and dissolved in chloroform and filtered. The solvent was removed by evaporation under reduced pressure and the solid product which remained was air dried. The 3,4,5-trichloro-N,N-dimethyl-2-(thiocyanomethyl)thio)benzenesulfonamide product was recovered in a yield of 0.7 grams (40 percent of theoretical) and melted at 155°-156° C.

WORKUP

后处理

  1. stirringthe mixture stirred at room temperature for 3 hours
  2. filtrationAt the end of this time period, the reaction mixture was filtered
  3. customto remove the solids which
  4. customhad precipitated
  5. temperatureafter cooling
  6. customthe solvent was reduced in volume by evaporation under reduced pressure
  7. customThe solids were thereafter removed by filtration
  8. filtrationAdditional filtrations
  9. customgave additional solids
  10. filtrationfiltered
  11. customThe solvent was removed by evaporation under reduced pressure
  12. customdried
  13. customThe 3,4,5-trichloro-N,N-dimethyl-2-(thiocyanomethyl)thio)benzenesulfonamide product was recovered in a yield of 0.7 grams (40 percent of theoretical) and melted at 155°-156° C.