Reaktion #64328

ord-e35f842b46234311aded068b70c38c4b

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITat room temperature for hr
  2. 2
    SonstigeThe reaction mixture was then evaporated under reduced pressure
  3. 3
    Sonstigethe crude product was chromatographed on silica-gel (25 g)
  4. 4
    WaschenElution with ether-hexane

Vorschrift

A solution of 1 -hexyl-3-hydroxymethyl-4-methoxy-6-methyl-2(1H)-quinolinone (Example 12, 0.6 g) in methylene chloride (12 ml) containing carbon tetrabromide (1 g) was treated with triphenylphosphine (0.87 g) and stirred at ice bath temperature for 5mins and then at room temperature for hr. The reaction mixture was then evaporated under reduced pressure and the crude product was chromatographed on silica-gel (25 g). Elution with ether-hexane gave 1-hexyl-3-bromomethyl-4-methoxy-6-methyl-2(1H)-quinolinone as a white crystralline solid. That the expected product was obtained was confirmed by the spectral data: MS: m/e 365,367 (M+); NMR (CDCl3): δ4.12 (s, 3H, OCH3) 4.68 (s, 2H, CH2Br).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05412104uspto-grants-1995_05