Reaktion #63366

ord-6b23019db7174762a1c14859947a9355

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONare then added dropwise
  2. 2
    SonstigeThe residue is partitioned between ethyl acetate and water
  3. 3
    Trocknenthe organic phase is dried over magnesium sulphate
  4. 4
    Einengenafter concentration
  5. 5
    Sonstigeby evaporation and subsequent recrystallisation from ethyl acetate/petroleum ether
  6. 6
    Sonstigethe product is obtained

Vorschrift

0.36 g of sodium hydride is added to a solution of 2.46 g of 1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione in 25 ml of N,N-dimethylformamide and the whole is stirred at room temperature for 30 minutes. 1.6 ml of n-butyl bromide dissolved in 10 ml of N,N-dimethylformamide are then added dropwise thereto. When the reaction is complete, the reaction mixture is freed of N,N-dimethylformamide. The residue is partitioned between ethyl acetate and water, and the organic phase is dried over magnesium sulphate and, after concentration by evaporation and subsequent recrystallisation from ethyl acetate/petroleum ether, the product is obtained having a melting point of 120°-123°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04764640uspto-grants-1988_08