Reaktion #812922

ord-a91496117935408cb635b5038161b98e

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigereaction at a temperature of 195° C. to 210° C. for 20 hours
  2. 2
    ExtraktionThe reaction product was then extracted with 140 ml of toluene
  3. 3
    SonstigeThe insoluble contents were removed by filtration
  4. 4
    EinengenThe filtrate was then concentrated
  5. 5
    workup.ADDITIONTo the concentrate was then added 120 ml of n-hexane
  6. 6
    Sonstigeto recover a crude crystal
  7. 7
    SonstigeThe crude crystal thus recovered
  8. 8
    Sonstigewas then purified by column chromatography (carrier: silica gel; elute: 1/2 mixture of toluene and n-hexane)

Vorschrift

8.66 g (0.021 mol) of N,N,N'-triphenylbenzidine thus obtained, 4.06 g (0.01 mol) of 4,4'-diiodobiphenyl, 2.90 g (0.021 mol) of anhydrous potassium carbonate, 0.32 g (0.005 mol) of copper powder, and 10 ml of nitrobenzene were mixed. The reaction mixture was then allowed to undergo reaction at a temperature of 195° C. to 210° C. for 20 hours. The reaction product was then extracted with 140 ml of toluene. The insoluble contents were removed by filtration. The filtrate was then concentrated. To the concentrate was then added 120 ml of n-hexane to recover a crude crystal. The crude crystal thus recovered was then purified by column chromatography (carrier: silica gel; elute: 1/2 mixture of toluene and n-hexane) to obtain 4.73 g (yield: 48.5%) of N,N'-bis(4'-diphenylamino-4-biphenylyl)-N,N'-diphenylbenzidine. The melting point of the product was from 242.5° C. to 243.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05707747uspto-grants-1998_01