Реакция #2307968

ord-dac9856803634a629a47771f26055a76

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураMixture heated
  2. 2
    Температураat reflux for 2 days
  3. 3
    ТемператураAfter cooling
  4. 4
    Другоеtoluene removed by rotary evaporation

Методика

9-bromo-10-(2-naphthylenyl)anthracene (3.3 g, 0.008 mol), diphenylamine (1.5 g, 0.008 mol), 1.0 g sodium tert-butoxide, 0.1 g palladium(II) acetate, 3 drops tri-tert-butylphosphine and 80 ml toluene are added to a round bottom flask under a nitrogen atmosphere. Mixture heated at reflux for 2 days. After cooling, toluene removed by rotary evaporation and remaining solid chromatographer on a silica gel column to yield 4.0 g (99% yield) of pure yellow product. FD-MS (m/z): 471.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07368178B2uspto-grants-2008_05