Reaktion #1503054

ord-ea1bae5e048f4e3eb7f2daab02439966

Reaktionsgleichung

CCOC(=O)/N=N/C(=O)OCC
diethylazodicarboxylate
C=C1CC[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@@H]12
dihydrocholesterol
O=C1NC(=O)c2ccccc21
phthalimide
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
3-phthalimidocholestane
Ausbeute 81.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONUpon the completion of addition the reaction mixture
  2. 2
    EinengenThe reaction mixture was concentrated in vacuo to a residue
  3. 3
    workup.DISSOLUTIONThis residue was dissolved in 50 ml hexane/ethyl acetate 95/5
  4. 4
    Sonstigea precipitate formed
  5. 5
    FiltrationThe mixture was filtered
  6. 6
    EinengenThe filtrate was concentrated to dryness in vacuo
  7. 7
    workup.DISSOLUTIONdissolved in 25 ml of hexane/ethyl acetate 95/5
  8. 8
    Sonstigechromatographed on 200 g silica gel (eluent 2 L hexane/ethyl acetate 95/5

Vorschrift

To a solution of dihydrocholesterol (5.0 g, 12.9 mmol, Aldrich), phthalimide (2.0 g, 13.6 mmol, Aldrich), and triphenylphosphine (3.8 g, 13.6 mmol, Aldrich) in THF (20 ml, Aldrich) stirred at 0° C. under a nitrogen atmosphere was added dropwise diethylazodicarboxylate (2.3 ml, 14.5 mmol, Aldrich). Upon the completion of addition the reaction mixture was allowed to warm to ambient temperature and stirred overnight. The reaction mixture was concentrated in vacuo to a residue. This residue was dissolved in 50 ml hexane/ethyl acetate 95/5 and a precipitate formed. The mixture was filtered. The filtrate was concentrated to dryness in vacuo, dissolved in 25 ml of hexane/ethyl acetate 95/5 and chromatographed on 200 g silica gel (eluent 2 L hexane/ethyl acetate 95/5 then 1 L hexane/ethyl acetate 90/10). A 76% yield of the desired 3-phthalimidocholestane (5.43 g) was obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05910487uspto-grants-1999_06