Reacción #338936

ord-375257fa85024251a427f14ca938deb1

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter completion of the addition
  2. 2
    OtroThe solvent is evaporated under reduced pressure
  3. 3
    Filtraciónthe precipitate is filtered
  4. 4
    Lavadowashed with 1:1 ether-hexane
  5. 5
    Otrodried
  6. 6
    OtroCrystallization from benzene

Procedimiento

Pentacene-maleimide adduct (5c) (375 mg, 1 mmole) are added to a solution of triphenyl phosphine (393 mg, 1.5 mmole) and 11-bromo-1-undecanol (375 mg, 1.5 mmole) in 40 mL of anhydrous tetrahydrofuran. To this mixture a solution of diisopropyl azodicarboxylate (300 mg, 1.5 mmole) in 1.0 mL of anhydrous THF is added dropwise under a stream of nitrogen. After completion of the addition, the solution is stirred at room temperature for 18 hours. The solvent is evaporated under reduced pressure and the residue is titrated with diethyl ether and the precipitate is filtered, washed with 1:1 ether-hexane and dried. Crystallization from benzene affords the pure sample of 11-bromoundecylmaleimide-pentacene adduct 5d.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07867469B2uspto-grants-2011_01