Reaktion #63368

ord-cfd4e181b30a4e3d94255ea376cfb65c

Reaktionsgleichung

CCCCCC.CCOC(C)=O
ethyl acetate hexane
[H-].[Na+]
sodium hydride
O=C1NC(=O)C2(c3ccc([N+](=O)[O-])cc3)CC1C2
1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione
CC(C)CI
isobutyl iodide
CC(C)CN1C(=O)C2CC(c3ccc([N+](=O)[O-])cc3)(C2)C1=O
3-isobutyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione

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 purification by chromatography over silica gel in the system ethyl acetate/hexane 1:2
  6. 6
    Sonstigethe product is obtained in the form of a solid

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. 2.76 g of isobutyl iodide 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 purification by chromatography over silica gel in the system ethyl acetate/hexane 1:2, the product is obtained in the form of a solid. Melting point 136°-137°. Rf (ethyl acetate/hexane 4:1)=0.6.

Quelle

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