反応 #481594

ord-237bc96903554e8db12240565a2768d7

反応方程式

CCc1ccc2c(c1)C(=O)c1ccccc1C2=O
2-ethylanthraquinone
O=C1CCC(=O)N1Br
NBS
O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoyl peroxide
CC(Br)c1ccc2c(c1)C(=O)c1ccccc1C2=O
2-(1-bromoethyl)-anthraquinone

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux for 1.5 hours
  2. 2
    温度On cooling
  3. 3
    ろ過the precipitate is collected by filtration
  4. 4
    洗浄washed on the
  5. 5
    ろ過filter with ethanol, hot water and finally ethanol again
  6. 6
    その他After drying
  7. 7
    その他this may be used without further purification (i.e. recrystallisation from benzene/methanol (1:1))

実験手順

A mixture of 2-ethylanthraquinone (25 Kg, 105.9 mol), NBS (19.1 Kg, 107.3 mol) and benzoyl peroxide (70%, 200 g, 0.58 mol) in CCl4 (˜150L) is stirred at reflux for 1.5 hours. On cooling, the precipitate is collected by filtration and washed on the filter with ethanol, hot water and finally ethanol again. After drying, this may be used without further purification (i.e. recrystallisation from benzene/methanol (1:1)).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06601732B1uspto-grants-2003_08