Reacción #481594

ord-237bc96903554e8db12240565a2768d7

Ecuación de reacción

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

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 1.5 hours
  2. 2
    TemperaturaOn cooling
  3. 3
    Filtraciónthe precipitate is collected by filtration
  4. 4
    Lavadowashed on the
  5. 5
    Filtraciónfilter with ethanol, hot water and finally ethanol again
  6. 6
    OtroAfter drying
  7. 7
    Otrothis may be used without further purification (i.e. recrystallisation from benzene/methanol (1:1))

Procedimiento

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)).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06601732B1uspto-grants-2003_08