Реакция #47189

ord-540cb1eae3d04860861ade46f9648f87

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеis taken in a round bottom flask
  2. 2
    ТемператураThe mixture is refluxed for 6 hrs under Dean Stark apparatus
  3. 3
    ДругоеAfter completion of the reaction (observed by TLC and by GC analysis)
  4. 4
    Фильтрацияthe reaction mixture is filtered
  5. 5
    Промывкаwashed with ethylacetate (5 ml×2)
  6. 6
    КонцентрированиеConcentrate the filtrate under reduced pressure
  7. 7
    Другоеthe crude product thus obtained
  8. 8
    Промывкаeluted with diethyl ether

Методика

A homogeneous mixture containing cinnamaldehyde (7.5 mmol), DDQ (11.3 mmol), BuOH (10 mL) and toluene (15 mL) is taken in a round bottom flask and catalytic amount of AMBERLYST® 15 (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 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. Butyl cinnamate (from formula I where X1═H, X2═H, X3═H, X4═H, X5═H, R═C4H9) is isolated in 94% yield. 1H-NMR (CDCl3, 300 MHz) δ7.48 (1H, d), 7.25 (2H, m), 7.11 (3H, m), 6.23 (1H, m), 3.98 (2H, t), 1.45 (2H, m), 1.19 (2H, m), 0.74 (3H, t); 13C-NMR (CDCl3, 75.4 MHz) δ166.5, 144.2, 134.4, 129.9, 127.9, 118.2, 64.0, 30.7, 19.1, 13.6.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07741508B2uspto-grants-2010_06