反応 #47184

ord-3f10c52917e242f1b549d3d2b543a9fc

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他is taken in a round bottom flask
  2. 2
    温度The mixture is refluxed for 6 hrs under Dean Stark apparatus
  3. 3
    その他After completion of the reaction (observed by TLC and by GC analysis)
  4. 4
    ろ過the reaction mixture is filtered
  5. 5
    洗浄washed with MeOH (5 ml×2)
  6. 6
    濃縮Concentrate the filtrate under reduced pressure
  7. 7
    その他the crude product thus obtained
  8. 8
    洗浄eluted with diethyl ether

実験手順

A homogeneous mixture containing 4-methoxycinnamaldehyde (7.5 mmol), DDQ (11.3 mmol), MeOH (15 mL) and toluene (10 mL) is taken in a round bottom flask and catalytic amount of AMBERLITE® IR 400 (0.1 g) is added to it. The mixture is refluxed for 6 hrs under Dean Stark apparatus. After completion of the reaction (observed by TLC and by GC analysis), the reaction mixture is filtered and washed with MeOH (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. Methyl 4-methoxycinnamate (from formula I where X1═H, X2═H, X3═OCH3, X4═H, X5═H, R═CH3) is isolated in 91% yield. 1H-NMR (CDCl3, 300 MHz) δ7.56 (1H, d, J=16.55 Hz), 7.37 (2H, d), 6.80 (2H, d), 6.22 (1H, d, J=16.55 Hz), 3.73 (3H, s), 3.70 (3H, s); 13C-NMR (CDCl3, 75.4 MHz) δ167.7, 161.4, 144.5, 129.7, 127.1, 115.2, 114.3, 55.3, 51.5.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07741508B2uspto-grants-2010_06