Reaktion #162256

ord-bc715d726b214670b8b515c9efd95368

Reaktionsgleichung

Nc1ccc(-c2ccccc2)cc1-c1ccccc1
2,4-diphenylaniline
Fc1ccccc1Br
1-bromo-2-fluorobenzene
[Na]
sodium
Fc1ccccc1Nc1ccc(-c2ccccc2)cc1-c1ccccc1
2,4-diphenyl-N-2-fluorophenylbenzenamine
Ausbeute 61.9%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeis removed
  2. 2
    ExtraktionThe reaction mixture is extracted with dichloromethane and water
  3. 3
    workup.DISTILLATIONbeing distilled under reduced pressure
  4. 4
    FiltrationThe resulting residence is filtered by silica gel column
  5. 5
    workup.DISTILLATIONdistilled under reduced pressure again
  6. 6
    SonstigeNext, by re-crystallizing
  7. 7
    Filtrationfiltering with dichloromethane and petroleum ether

Vorschrift

2,4-diphenylaniline (12 mmol), 1-bromo-2-fluorobenzene (10 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.15 mmol), (±)-2,2′-bis(diphenylphosphine)-1,1′-binaphthalene (0.3 mmol) and sodium tert-butoxie (14 mmol) are put in a two-neck round-bottom flask and dissolved in toluene (30 mL). Subsequently, the resulting solution is stirred in a bath under a temperature of about 100° C. for 24 hours. After completion of the reaction, toluene is removed. The reaction mixture is extracted with dichloromethane and water, and then being distilled under reduced pressure. The resulting residence is filtered by silica gel column and distilled under reduced pressure again. Next, by re-crystallizing and filtering with dichloromethane and petroleum ether, 2,4-diphenyl-N-2-fluorophenylbenzenamine (2.1 g) is yielded.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08835020B2uspto-grants-2014_09