HRID1110850

反应详情

EQUATION

反应方程式

HRID 1110850 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A suspension of 13.36 g of 1-methyl-beta-oxo-alpha-(phenylcarbamoyl)-2-pyrrolepropionitrile and 6.06 g of tromethamine in 100 ml of ethanol is heated to reflux for about one half hour, the solution is allowed to cool to about room temperature, treated with activated charcoal, filtered and reduced to a volume of about 45 ml at a temperature below 60°. The solution is heated to about 50°-55°, 100 ml of toluene is slowly added over a period of about one half hour with stirring and the resulting mixture is slowly cooled to about 15° over a period of one hour and stirred at 15° about 1 hour. The resulting crystalline product is collected by filtration, washed with toluene and dried at 70°-80° under low vacuum for 24 hours to yield 1-methyl-beta-oxo-alpha-(phenylcarbamoyl)-2-pyrrolepropionitrile tromethamine salt of Example 1. Second crop can be obtained by evaporating mother liquor to dryness and crystallizing more product from ethanol: toluene (1:2) as described above.

WORKUP

后处理

  1. temperatureis heated
  2. temperatureto reflux for about one half hour
  3. temperatureto cool to about room temperature
  4. filtrationfiltered
  5. customreduced to a volume of about 45 ml at a temperature below 60°
  6. temperatureThe solution is heated to about 50°-55°
  7. addition100 ml of toluene is slowly added over a period of about one half hour
  8. temperaturethe resulting mixture is slowly cooled to about 15° over a period of one hour
  9. stirringstirred at 15° about 1 hour
  10. filtrationThe resulting crystalline product is collected by filtration
  11. washwashed with toluene
  12. customdried at 70°-80° under low vacuum for 24 hours