Реакция #2044

ord-34a870e6034145a8adf96361ff614be2

Растворители

Условия реакции

Температура
200°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISSOLUTIONto dissolve a product
  2. 2
    Фильтрацияthe resultant mixture was filtrated
  3. 3
    Концентрированиеconcentrated
  4. 4
    ДругоеThe concentrated product was purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4)

Методика

33.85 g (0.2 mol) of 5-aminoacenaphtthene was mixed with 102.1 g (0.5 mol) of iodo benzene, 1.3 g (0.02 mol) of copper powder, 34.5 g (0.25 mol) of anhydrous potassium carbonate and 100 ml of nitrobenzene, and the mixture was stirred at 200° C. for 26 hours. The reaction was determined to be finished when disappearance of 5-aminoacenaphthene and 5-(N-phenylamino)acenaphthene as an intermediate was identified. 300 ml of toluene was added thereto to dissolve a product, and the resultant mixture was filtrated and concentrated. The concentrated product was purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4) to obtain 48.7 g (yield: 75.7%, melting point: 168.5°-170.5° C.) of 5-(N,N-diphenylamino)acenaphthene.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05728500uspto-grants-1998_03