Reaktion #70673

ord-e6054a3a14fb43a2bff01a7ca1b28c62

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA clean and dry 500 ml round bottom flask
  2. 2
    Sonstigeequipped with a reflux condenser, magnetic stir bar
  3. 3
    Sonstigethermometer with adapter was prepared
  4. 4
    Sonstigepurged with nitrogen Anhydrous toluene (250.0 ml)
  5. 5
    Sonstigewas transferred to this flask by cannula
  6. 6
    SonstigeThe reaction solution was purged with a strong nitrogen flow for 30 minutes
  7. 7
    TemperaturThe vessel was heated
  8. 8
    Temperaturto reflux for approximately 5 hours
  9. 9
    Filtrationfiltered through a Celite and silica gel pad
  10. 10
    Waschenwashing thoroughly with acetone and chloroform
  11. 11
    SonstigeSolvent was removed by rotary evaporation
  12. 12
    SonstigeThe crude material was purified by flash column chromatography

Vorschrift

A clean and dry 500 ml round bottom flask equipped with a reflux condenser, magnetic stir bar, and thermometer with adapter was prepared and purged with nitrogen Anhydrous toluene (250.0 ml) was transferred to this flask by cannula. 2-(3-bromophenyl)-1,3-dioxolane (6.0 ml, 0.0397 mol) was added by syringe followed by the manual addition of 1-naphthylamine (5.08 g, 0.0355 mol). The reaction solution was purged with a strong nitrogen flow for 30 minutes. Sodium tert-butoxide (5.60 g, 0.0583 mol) and Pd2dba3 (0.65 g, 0.0007 mol) were then added manually, followed by the addition of tri-tert-butylphosphine (1.30 g, 0.0064 mol) in toluene (˜10 ml) via syringe. The vessel was heated to reflux for approximately 5 hours. The reaction was then cooled to room temperature and filtered through a Celite and silica gel pad washing thoroughly with acetone and chloroform. Solvent was removed by rotary evaporation. The crude material was purified by flash column chromatography using ethyl acetate/hexane as an eluent. This provided pure product confirmed by NMR spectroscopy.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08535974B2uspto-grants-2013_09