Reaktion #2207345

ord-13b71330ccda4d47a8f0c4453f84fbf0

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe cooling bath is removed
  2. 2
    SonstigeThe reaction mixture is then partitioned between saturated aqueous NaHCO3 solution and Et2O
  3. 3
    SonstigeThe organic phase is separated
  4. 4
    Waschenwashed with brine
  5. 5
    Trocknendried over MgSO4
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated in vacuo

Vorschrift

80 mL (0.67 mmol) of PBr3 is added slowly to a solution of 104 mg (0.57 mmol) of (4-methyl-2-phenyl-oxazol-5-yl)-methanol in 0.5 mL of Et2O and 1.5 mL of CH2Cl2 at 0° C. The cooling bath is removed, and the reaction mixture is stirred for 4 h. The reaction mixture is then partitioned between saturated aqueous NaHCO3 solution and Et2O. The organic phase is separated and washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to produce 5-bromomethyl-4-methyl-2-phenyl-oxazole as a solid; 1H NMR (250 MHz, CDCl3) δ7.90-7.99 (m, 2H), 7.32-7.40 (m, 3H), 4.50 (s, 2H), 2.16 (s, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06689801B2uspto-grants-2004_02