Reaktion #514607

ord-62916b7ce4a346b997cf4cbd4f19b592

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe mixture was then reacted for 6 hours
  2. 2
    Einengenconcentrated under reduced pressure
  3. 3
    WaschenThe organic phase was washed with brine
  4. 4
    Trocknendried over Na2SO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated under reduced pressure
  7. 7
    Sonstigeto produce a solid which
  8. 8
    Sonstigewas purified by column chromatography (silica gel

Vorschrift

Norglaucine (1.90 g, 5.2 mmol), methanol (50 ml) and 35.5% formaldehyde (6.0 ml) were successively placed in a 250 ml reaction bottle. To the mixture, NaBH4 was added portionwise (total 2.0 g, 52 mmol) at room temperature while stirring. The mixture was then reacted for 6 hours, concentrated under reduced pressure, and fractionated between water (150 ml) and chloroform (150 ml×3). The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to produce a solid which was purified by column chromatography (silica gel, with chloroform as the eluant) to obtain solid product glaucine (1.78 g, 90%). Physical data were as follows: mp: 112-114° C. (diethyl ether); [α]D24 +120.0° (c=0.30, MeOH); 1H NMR (CDCl3, 400 MHz) δ 8.06 (1H, s, H-11), 6.75 (1H, s, H-8), 6.56 (1H, s, H-3), 3.91 (3H, s, 9-OMe), 3.88 (3H, s, 10-OMe), 3.86 (3H, s, 2-OMe), 3.64 (3H, s, 1-OMe), 2.54 (3H, s, N-Me).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06313134B1uspto-grants-2001_11