反应 #465947

ord-4ce61dce3eda489db03443a0dde07896

反应方程式

O=C1CCC(=O)N1Br
N-bromosuccinimide
c1ccc(N(c2ccccc2)c2ccccc2)cc1
triphenylamine
Brc1ccc(N(c2ccccc2)c2ccccc2)cc1
4-bromotriphenylamine
收率 61.7%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Next, N,N-dimethylformamide was removed from the reaction
  2. 2
    萃取the resulting solid matter was extracted with carbon tetrachloride
  3. 3
    其他Then, carbon tetrachloride was removed
  4. 4
    其他the reaction product was recrystallized twice from ethanol

实验过程

Into a 200 ml three-necked flask, 8.0 g (45 mmol) of N-bromosuccinimide and 10.0 g (41 mmol) of triphenylamine were placed, followed by 150 ml of N,N-dimethylformamide. The mixture was stirred overnight at room temperature. Next, N,N-dimethylformamide was removed from the reaction, and the resulting solid matter was extracted with carbon tetrachloride. Then, carbon tetrachloride was removed, and the reaction product was recrystallized twice from ethanol to give a white solid, 4-bromotriphenylamine in an amount of 8.2 g (yield: 61.7%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06296978B1uspto-grants-2001_10