Reacción #480324

ord-da338871b686470f8defd2376acba51b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroobtained in this way
  2. 2
    Otrothe mixture is reacted for 30 hours at 200° C
  3. 3
    Lavadothe reactant is eluted with chloroform
  4. 4
    OtroThereafter, the resultant substance is purified in accordance with a usual method
  5. 5
    Otrois synthesized

Procedimiento

Naphthacenonaphthacene is dissolved in carbon tetrachloride. While the resultant mixture is cooled, 1 mol equivalent of bromine is added thereto. The mixture is reacted for 4 hours and brominated. Thereafter, the mixture is purified in accordance with a usual method, and 6,13-dibromonaphthacenonaphthacene is obtained. Diphenylamine, potassium carbonate, and copper powder are added to the 6,13-dibromonaphthacenonaphthacene obtained in this way, and the mixture is reacted for 30 hours at 200° C. After the reaction solution is diluted with water, the reactant is eluted with chloroform. Thereafter, the resultant substance is purified in accordance with a usual method, and the 6,13-bis(diphenylamino)naphthacenonaphthacene represented by the following formula is synthesized. (Note that, in the formula, “Ph” represents a phenyl group.)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06805977B2uspto-grants-2004_10