反応 #6306

ord-5c4084f677714fefb5da04262b23b483

反応方程式

Cc1ccc(-c2nc3ccccc3o2)cc1
2-(4-methylphenyl)benzoxazole
O=C1CCC(=O)N1Br
N-bromosuccinimide
O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoyl peroxide
BrCc1ccc(-c2nc3ccccc3o2)cc1
2-(4-Bromomethylphenyl)benzoxazole

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux for 20 hours
  2. 2
    その他the solid byproducts are removed by filtration
  3. 3
    濃縮The filtrate is concentrated in vacuo
  4. 4
    その他the product is purified by recrystallization from benzene

実験手順

A stirred solution of 20.9 g (0.1 mole) of 2-(4-methylphenyl)benzoxazole, 17.8 g (0.1 mole) of N-bromosuccinimide, and 0.4 g (0.2 mole %) of benzoyl peroxide in carbon tetrachloride is heated at reflux for 20 hours. After cooling to room temperature, the reaction is diluted by the addition of carbon tetrachloride, and the solid byproducts are removed by filtration. The filtrate is concentrated in vacuo, and the product is purified by recrystallization from benzene.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05247042uspto-grants-1993_09