Reaktion #996327

ord-d9c535e88f1842be8a4845c4e82941a0

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigereaction
  2. 2
    Extraktionthe aqueous layer was extracted with Et2O (2×)
  3. 3
    Waschenthe combined organic layers were washed sequentially with 10% HCl (3×), saturated NaHCO3 (2×), H2O (2×) and brine
  4. 4
    Trocknendried over anhydrous Na2SO4
  5. 5
    EinengenAfter concentration, crude product purity
  6. 6
    SonstigeThe crude product (5p) was carried on to next step directly without subsequent purification

Vorschrift

To crude (4p), acetic anhydride (36.5 mL, 386.4 mmol) and pyridine (37.5 mL, 463.7 mmol) were added. The resulting mixture was stirred at room temperature for 18 hours, checked by HPLC the next day (reaction appeared mostly complete). The mixture was then poured onto cold H2O/Et2O, the aqueous layer was extracted with Et2O (2×), the combined organic layers were washed sequentially with 10% HCl (3×), saturated NaHCO3 (2×), H2O (2×) and brine, and then dried over anhydrous Na2SO4. After concentration, crude product purity was checked by thin-layer chromatography (hexane/ethyl acetate, 7:3) and HPLC. No mass ion was observed. The crude product (5p) was carried on to next step directly without subsequent purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08017641B2uspto-grants-2011_09