反応 #465947

ord-4ce61dce3eda489db03443a0dde07896

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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%).

出典

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