Réaction #1379893

ord-d2e16c03fbb44fcbbcc773d79ee779ea

Équation de réaction

NO
hydroxylamine
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butyldiphenylsilyl chloride
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
CNO.Cl
N-methyl hydroxylamine hydrochloride
CN(O)[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
N-Methyl,N-(tert-butyldiphenylsilyl)hydroxylamine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe two layers were separated
  2. 2
    Extractionthe aqueous layer was extracted with methylene chloride
  3. 3
    Séchagedried with magnesium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated to dryness under reduced pressure
  6. 6
    AutreThe resulting product was purified by liquid chromatography on silica gel using
  7. 7
    workup.ADDITIONa mixture of hexane and ethyl acetate
  8. 8
    Lavageto elute the desired product

Mode opératoire

One possible synthetic scheme for hydroxylamine derivatives involves adding tert-butyldiphenylsilyl chloride and N,N-diisopropylethylamine to a suspension of N-methyl hydroxylamine hydrochloride in dry dichloromethane. The reaction mixture was stirred followed by the addition of water. The two layers were separated and the aqueous layer was extracted with methylene chloride. The organic solutions were then combined, dried with magnesium sulfate, filtered, and concentrated to dryness under reduced pressure. The resulting product was purified by liquid chromatography on silica gel using a mixture of hexane and ethyl acetate to elute the desired product. The purification process gave N-Methyl,N-(tert-butyldiphenylsilyl)hydroxylamine (27).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07238339B2uspto-grants-2007_07