Reaktion #412258

ord-8c2f4a5b79ac43cd8f1135414d7ac940

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was refluxed
  2. 2
    Filtrationthe insoluble residue was filtered off
  3. 3
    Einengenthe filtrate was concentrated
  4. 4
    SonstigeThe crude product was purified by column chromatography (silica gel, mobile phase THF/methanol/ammonia 85/13/2)

Vorschrift

83.2 g (966 mmol) of piperazine, 38.0 g (339 mmol) of potassium tert-butoxide and 50.0 g (241 mmol) of 1-bromonaphthalene were added to a mixture of 5.4 g (24.2 mmol) of palladium acetate and 14.7 g (48.3 mmol) of tri-o-tolyl-phosphine in 500 ml of xylene, and the mixture was refluxed with efficient stirring under a nitrogen atomsphere for 10 h. The mixture was then diluted with methylene chloride, the insoluble residue was filtered off, and the filtrate was concentrated. The crude product was purified by column chromatography (silica gel, mobile phase THF/methanol/ammonia 85/13/2). 21.5 g (42%) of product with melting point 84-86° C. were isolated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06222034B1uspto-grants-2001_04