Reaktion #50244

ord-bc023ee232b849a4ba76f663d1c2ba20

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction is then quenched with saturated ammonium chloride
  2. 2
    Extraktionextracted several times with methylene chloride
  3. 3
    TrocknenThe combined organic layers are dried (MgSO4)
  4. 4
    Sonstigethe solvent is evaporated
  5. 5
    SonstigeThe product is purified by silica gel chromatography (20% ethyl acetate/hexane)

Vorschrift

Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate (0.98 g, 2.98 mmol) is dissolved in methylene chloride (50 mL), and boron trifluoride etherate (1.8 mL, 15 mmol) is added. The reaction is stirred at room temperature for 26 hours. The reaction is then quenched with saturated ammonium chloride and extracted several times with methylene chloride. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (20% ethyl acetate/hexane) to give ethyl 3-methylidene-2-oxo-1-azacyclodecane-10-carboxylate, m.p. 91°-92° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05426103uspto-grants-1995_06