Reaktion #68909

ord-e8c5a1c36f5d4ec695ceb777a2da6bf8

Reaktionsgleichung

O=[N+]([O-])c1cccc(S(=O)(=O)OC[C@@H]2CO2)c1
(S)-glycidyl 3-nitrobenzene sulfonate
Oc1cccc2[nH]c3ccccc3c12
9H-Carbazol-4-ol
[H-].[Na+]
NaH
c1ccc2c(c1)[nH]c1cccc(OC[C@@H]3CO3)c12
title compound
c1ccc2c(c1)[nH]c1cccc(OC[C@@H]3CO3)c12
(S)-4-Oxiranylmethoxy-9H-carbazole

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGwas then stirred at room temperature for 14 hours
  2. 2
    SonstigeThe reaction was quenched with NaHCO3 (saturated)
  3. 3
    Extraktionextracted with ethyl acetate (3×)
  4. 4
    TrocknenThe organic layer was dried with magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigethe solvent evaporated under reduced pressure
  7. 7
    Sonstigeto yield crude product which
  8. 8
    Sonstigewas purified by silica gel chromatography (60% Ethyl acetate/heptane)

Vorschrift

9H-Carbazol-4-ol (0.367 g, 2.0 mmol) was placed in a flask with DMF (10 mL) and NaH (60% dispersion in oil, 77 mg, 2.0 mmol) and stirred for 30 min at room temperature. (S)-glycidyl 3-nitrobenzene sulfonate (0.52 g, 2.0 mmol) was added to the reaction mixture, which was then stirred at room temperature for 14 hours. The reaction was quenched with NaHCO3 (saturated) and then extracted with ethyl acetate (3×). The organic layer was dried with magnesium sulfate, filtered and the solvent evaporated under reduced pressure to yield crude product which was purified by silica gel chromatography (60% Ethyl acetate/heptane) to yield the title compound as a residue.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530475B2uspto-grants-2013_09