Reaktion #5486

ord-457a83af2b8e486aa8de7028583f3486

Reaktionsgleichung

[NH4+].[OH-]
ammonium hydroxide
CS(=O)(=O)O
Methanesulfonic acid
CCOC(=O)C1CCCCCCCC1=O
2-Ethoxycarbonyl-cyclononanone
[N-]=[N+]=[N-].[Na+]
sodium azide
CCOC(=O)C1CCCCCCCC(=O)N1
ethyl 2-oxo-1-azacyclodecane-10-carboxylate

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    Temperaturheated
  2. 2
    Temperaturto reflux for 4 hours
  3. 3
    workup.ADDITIONThe reaction mixture is poured onto ice
  4. 4
    Extraktionextracted several times with methylene chloride
  5. 5
    TrocknenThe combined organic layers are dried (MgSO4)
  6. 6
    Sonstigethe solvent is evaporated
  7. 7
    SonstigeThe product is purified by silica gel chromatography (40% ethyl acetate/hexane)

Vorschrift

2-Ethoxycarbonyl-cyclononanone (13.72 g, 64.7 mmol) is dissolved in chloroform (200 mL) and cooled to 0° C. Methanesulfonic acid (62.4 g, 650 mmol) is added, followed by sodium azide (12.68 g, 195 mmol). The reaction is stirred at room temperature for 30 minutes, and then heated to reflux for 4 hours. The reaction mixture is poured onto ice, made basic with concentrated ammonium hydroxide (pH=9), 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 (40% ethyl acetate/hexane) to give ethyl 2-oxo-1-azacyclodecane-10-carboxylate, m.p. 101°-103° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05244889uspto-grants-1993_09