Reaktion #50241

ord-ae6e3feffc3748f18ceeb2c6741450df

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe reaction is stirred at 0° C. for 4 hours
  2. 2
    SonstigeThe reaction is quenched
  3. 3
    workup.ADDITIONby adding saturated sodium sulfite (until the color of excess bromine
  4. 4
    Extraktionextracted several times with methylene chloride
  5. 5
    TrocknenThe combined organic layers are dried (Na2SO4)
  6. 6
    Sonstigethe solvent is evaporated
  7. 7
    SonstigeThe product is purified by silica gel chromatography (15% ethyl acetate/hexane)

Vorschrift

Ethyl 2-oxo-1-azacyclodecane-10-carboxylate (4.0 g, 17.6 mmol) is dissolved in methylene chloride (50 mL), and cooled to 0° C. Phosphorus pentachloride (3.85 g, 18.5 mmol) and iodine (0.051 g, 0.2 mmol) are added. The reaction is stirred for 15 minutes at 0° C. Then, bromine (3.10 g, 19.4 mmol) is added, and the reaction is stirred at 0° C. for 4 hours. The reaction is quenched by adding saturated sodium sulfite (until the color of excess bromine disappears), and extracted several times with methylene chloride. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give cis ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate, m.p. 132°-134° C.

Quelle

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