HRID1981517

反应详情

EQUATION

反应方程式

HRID 1981517 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

40.75 g (0.1 mole) of 3-(4-trifluoromethylphenyl)-7-chloro-10-hydroxy-3,4-dihydroacridine-1,9(2H,10H)-dione are suspended in 500 ml of ethanol, 11.5 g (0.1 mole) of N-methyl-N'-aminopiperazine are added and the reaction mixture is heated to reflux for 30 minutes. A clear orange-red solution forms during this. After cooling down, the ethanol is distilled out in a rotary evaporator and the solid residue is recrystallized from toluene/cyclohexane (1:1). 43 g=85% of theory of the title compound is thus obtained in the form of orange-yellow crystals of melting point 213° C.

WORKUP

后处理

  1. temperaturethe reaction mixture is heated
  2. temperatureto reflux for 30 minutes
  3. temperatureAfter cooling down
  4. distillationthe ethanol is distilled out in a rotary evaporator
  5. customthe solid residue is recrystallized from toluene/cyclohexane (1:1)