Reaktion #340538

ord-70f79245a8654bb08483f65b51182e6c

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenthe mixture is washed three times with 15 ml of ethyl acetate
  2. 2
    TrocknenThe organic phase is dried over magnesium sulfate
  3. 3
    Sonstigethe solvent is then removed under reduced pressure
  4. 4
    SonstigeThe residue is purified by RP-HPLC

Vorschrift

2 g of the 3-[2-(4-fluorophenyl)-5-methyloxazol-4-ylmethoxy)cyclohexanol are dissolved in 15 ml of dimethylformamide, and 0.3 g of sodium hydride is added. After 30 minutes, 2.4 g of allyl bromide are added dropwise. The mixture is stirred at room temperature for 5 hours. 15 ml of 1N HCl are then added to the reaction mixture, and the mixture is washed three times with 15 ml of ethyl acetate. The organic phase is dried over magnesium sulfate and the solvent is then removed under reduced pressure. The residue is purified by RP-HPLC. This gives 2.4 g of 4-(3-allyloxycyclohexyloxymethyl)-2-(4-fluorophenyl)-5-methyloxazole as a yellowish oil. C20H24FNO3 (345.42) MS (ESI): 346 (M+H+)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07872034B2uspto-grants-2011_01