反应 #2314311

ord-209cf0c949fc41748cfdaadaadb31293

反应方程式

Nc1ccccc1N
o-phenylenediamine
O=C1OC(=O)C2(c3ccccc3)C(c3ccccc3)=C(c3ccccc3)C=CC12c1ccccc1
1,2,3,4-tetraphenylphthalic anhydride
CC(=O)O
acetic acid
O=C1c2c(-c3ccccc3)c(-c3ccccc3)c(-c3ccccc3)c(-c3ccccc3)c2-c2nc3ccccc3n21
yellow solid
O=C1c2c(-c3ccccc3)c(-c3ccccc3)c(-c3ccccc3)c(-c3ccccc3)c2-c2nc3ccccc3n21
1,2,3,4-tetraphenyl-benzo [4,5] imidazo [2,1-a] isoindol-11-one

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他A 500 ml round-bottom flask equipped with a stirrer
  2. 2
    温度reflux condenser
  3. 3
    温度heated
  4. 4
    温度at reflux for 11 hours
  5. 5
    温度The slurry is cooled
  6. 6
    其他the yellow solid is isolated by filtration
  7. 7
    洗涤The solid is washed with water

实验过程

A 500 ml round-bottom flask equipped with a stirrer and reflux condenser is charged with 8.34 g (73.3 mmol) of o-phenylenediamine (95%), 33.0 g (66.3 mmol) of 1,2,3,4-tetraphenylphthalic anhydride, and 200 ml of glacial acetic acid. Under nitrogen atmosphere, the mixture is stirred and heated at reflux for 11 hours. The slurry is cooled and the yellow solid is isolated by filtration. The solid is washed with water and then with methanol. 35.1 g of an yellow solid is obtained (92%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06413655B2uspto-grants-2002_07