反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
In a 500 ml 4-necked flask, were poured 71.15 g (355 mmol) of tetrafluorophthalonitrile, 2.16 g (37.1 mmol) of potassium fluoride and 210 g of acetonitrile, and resulting was heated to 80° C. This mixture was kept at 80° C. with stirring, and to this mixture were dropped 4.40 g (17.7 mmol) of tetrachlorohydroquinone in 200 ml of acetonitrile over 1 hour. After dropping, reaction was performed at 80° C. for 6 hours. The reaction solution was cooled, filtrated, and the resulting residue washed with 30 ml and 15 ml of acetonitrile. After the filtrate had been concentrated on an evaporator to remove the solvent, 62.34 g of tetrafluorophthalonitrile was removed under in vacuo. To this was poured 27 ml of toluene and reflux performed for 1 hour. After cooling, the residue was washed with 5 ml, 25 ml and 5 ml of toluene, respectively, and further 12 ml of deionized water for three times. Finally, by drying the residue at 70° C. in vacuo, 9.08 g of 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene were obtained (yield: 84%).
WORKUP
后处理
- customresulting
- customwas kept at 80° C.
- customreaction
- temperatureThe reaction solution was cooled
- filtrationfiltrated
- washthe resulting residue washed with 30 ml and 15 ml of acetonitrile
- concentrationAfter the filtrate had been concentrated on an evaporator
- customto remove the solvent, 62.34 g of tetrafluorophthalonitrile
- customwas removed under in vacuo
- additionTo this was poured 27 ml of toluene
- temperaturereflux
- waitperformed for 1 hour
- temperatureAfter cooling
- washthe residue was washed with 5 ml, 25 ml and 5 ml of toluene
- customFinally, by drying the residue at 70° C. in vacuo