Réaction #6688

ord-0e36fea0a7614a60a1024966a981a2e5

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with ethyl acetate:hexane(1:1)
  2. 2
    Lavagewashed with brine
  3. 3
    Séchagedried over MgSO4
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    AutreThe purification by chromatography
  6. 6
    Autreon silica gel (5% EtOAc/hexanes) and recrystallization from acetonitrile

Mode opératoire

A biphasic solution of 2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid (25): (1 equi.), 4-bromo-benzoic acid ethyl ester (12), (1 equi.), sodium carbonate (2.7 equi.), and Pd(PPh3)4 catalyst (0.01 equi.) in water-toluene (1:1) (2 mL/mmole) was stirred at 100 C. temperature for 12 h., cooled to room temperature, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. The purification by chromatography on silica gel (5% EtOAc/hexanes) and recrystallization from acetonitrile afforded 2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester (26) as a white solid (88%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07083832B2uspto-grants-2006_08