Reaktion #47182

ord-1c1b94d5de364e8f806bcfb2b478fa2f

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeis taken in a round bottom flask
  2. 2
    workup.ADDITIONcatalytic amount of silica gel (0.1 g) is added to it
  3. 3
    SonstigeAfter completion of the reaction (observed by TLC and by GC analysis)
  4. 4
    Filtrationthe reaction mixture is filtered
  5. 5
    Waschenwashed with ethylacetate (5 ml×2)
  6. 6
    EinengenConcentrate the filtrate under reduced pressure
  7. 7
    Sonstigethe crude product thus obtained
  8. 8
    Wascheneluted with diethyl ether

Vorschrift

A homogeneous mixture containing cinnamaldehyde (7.5 mmol), Chloronil (22.5 mmol), isopropanol (10 mL) is taken in a round bottom flask and catalytic amount of silica gel (0.1 g) is added to it. The mixture is stirred for 20 hrs at room temperature. After completion of the reaction (observed by TLC and by GC analysis), the reaction mixture is filtered and washed with ethylacetate (5 ml×2). Concentrate the filtrate under reduced pressure and the crude product thus obtained is loaded on a neutral alumina column and eluted with diethyl ether. Isopropyl cinnamate (from formula I where X1═H, X2═H, X3═H, X4═H, X5═H, R═C3H8) is isolated in 49% yield. 1H-NMR (CDCl3, 300 MHz) δ7.59 (1H, d, J=16.55 Hz), 7.41 (2H, m), 7.27 (3H, m), 6.34 (1H, d, J=16.55 Hz), 5.07 (1H, m), 1.18 (6H, d); 13C-NMR (CDCl3, 75.4 MHz) δ166.4, 144.3, 134.5, 130.1, 128.6, 128.0, 118.8, 67.7, 21.9.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741508B2uspto-grants-2010_06