반응 #481594

ord-237bc96903554e8db12240565a2768d7

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 1.5 hours
  2. 2
    온도On cooling
  3. 3
    여과the precipitate is collected by filtration
  4. 4
    세척washed on the
  5. 5
    여과filter with ethanol, hot water and finally ethanol again
  6. 6
    기타After drying
  7. 7
    기타this may be used without further purification (i.e. recrystallisation from benzene/methanol (1:1))

실험 절차

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)).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06601732B1uspto-grants-2003_08