HRID264711

反应详情

EQUATION

反应方程式

HRID 264711 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

9.6 g (0.24 mol) of 60% sodium hydride and 150 ml of N,N-dimethylformamide were placed in a container equipped with a stirrer, a reflux condenser and a nitrogen-introducing tube, and the solution was then stirred under the feed of nitrogen. Afterward, 35 g (0.25 mol) of 3,5-dimethyl-1,6-heptadiene-4-ol was added dropwise thereto at 20°-30° C. over 1 hour, and the solution was then stirred at the same temperature for 3 hours to prepare a sodium alcoholate solution. Next, 34.6 g (0.2 mol) of 3-nitrophthalonitrile and 150 ml of N,N-dimethylformamide were placed in a container equipped with a stirrer, and the above-mentioned sodium alcoholate solution was added dropwise thereto at 0° C. or less over 5 hours. After completion of the addition, the temperature of the solution was raised up to a level of 20°-30° C., and the solution was then stirred for 3 hours to bring reaction to an end. The thus obtained reaction solution was poured into 3 l of water and then stirred for 30 minutes, and 500 ml of toluene were added. After stirring for 30 minutes, the resulting toluene layer was separated. After toluene was distilled off under reduced pressure, recrystallization was carried out from 600 ml of n-hexane to obtain 44.7 g of 3-(3,5-dimethyl-1,6-heptadiene-4-oxy)phthalonitrile (yield=84.0%).

WORKUP

后处理

  1. customequipped with a stirrer, a reflux condenser
  2. additiona nitrogen-introducing tube
  3. stirringthe solution was then stirred at the same temperature for 3 hours
  4. customequipped with a stirrer
  5. waitat 0° C. or less over 5 hours
  6. additionAfter completion of the addition
  7. temperaturethe temperature of the solution was raised up to a level of 20°-30° C.
  8. stirringthe solution was then stirred for 3 hours
  9. customreaction to an end
  10. customThe thus obtained reaction solution
  11. stirringstirred for 30 minutes
  12. stirringAfter stirring for 30 minutes
  13. customthe resulting toluene layer was separated
  14. distillationAfter toluene was distilled off under reduced pressure, recrystallization