反应详情

Successively, 450 g of the obtained 1,2,4,5-cyclohexanetetracarboxylic acid and 4000 g of acetic anhydride were charged into a 5-L glass separable flask equipped with a Dimroth condenser. The inner atmosphere of the reactor was replaced with nitrogen gas under stirring. The temperature was raised to the refluxing temperature of the solvent to allow the solvent to reflux for 10 min. Thereafter, the temperature was lowered to room temperature under stirring to precipitate crystals. The precipitated crystals were separated by solid-liquid separation and dried to obtain primary crystals. The mother liquor after separation was concentrated under reduced pressure using a rotary evaporator to precipitate crystals. The precipitated crystals were separated by solid-liquid separation and dried to obtain secondary crystals. In total of the primary and secondary crystals, 375 g of 1,2,4,5-cyclohexanetetracarboxylic dianhydride was obtained (yield of anhydration: 96.6%).

1. customequipped with a Dimroth condenser
2. temperatureThe temperature was raised to the refluxing temperature of the solvent
3. temperatureto reflux for 10 min
4. customwas lowered to room temperature
5. stirringunder stirring
6. customto precipitate crystals
7. customThe precipitated crystals were separated by solid-liquid separation
8. customdried
9. customto obtain primary crystals
10. customThe mother liquor after separation
11. concentrationwas concentrated under reduced pressure
12. customa rotary evaporator
13. customto precipitate crystals
14. customThe precipitated crystals were separated by solid-liquid separation
15. customdried
16. customto obtain secondary crystals