Reaktion #60347

ord-91a8661e4ce5415794b20c22b66ec1ea

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was heated slowly
  2. 2
    Temperaturto reflux for 4 h
  3. 3
    SonstigeThe layers were separated
  4. 4
    Extraktionthe aqueous layer was extracted with EtOAc until tlc analysis of the aqueous layer
  5. 5
    TrocknenThe combined organics were dried over MgSO4
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    Sonstigeto furnish the crude material, which
  8. 8
    Sonstigewas purified by flash column chromatography

Vorschrift

LAH (6.35 g, 167 mmol) was suspended in THF (100 mL) at 0° C. A solution of chroman-4-one oxime (Step A) (10.92 g, 66.92 mmol) in THF (100 mL) was added drop-wise. The mixture was heated slowly to reflux for 4 h. The reaction was cooled to RT and added drop-wise to a stirred saturated solution of Rochelle's salt in H2O. The bi-phasic mixture was stirred rapidly at RT for 1 h. The layers were separated and the aqueous layer was extracted with EtOAc until tlc analysis of the aqueous layer showed no evidence of the title compound. The combined organics were dried over MgSO4 and concentrated in vacuo to furnish the crude material, which was purified by flash column chromatography to afford the title compound. MS (APCI pos) 150 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07425631B2uspto-grants-2008_09