Реакция #47193

ord-7153c88da5ed49fda3985f95cd9b739e

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), ethylene glycol (10 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. 2-Hydroxyethyl cinnamate (from formula I where X1═H, X2═H, X3═H, X4═H, X5═H, R═C2H5O) is isolated in 88% yield. 1H-NMR (CDCl3, 300 MHz) δ7.65 (1H, d, J=16.55 Hz), 7.42 (2H, m), 7.29 (3H, m), 6.38 (1H, d, J=16.55 Hz), 4.37 (2H, t), 3.66 (2H, t); 13C-NMR (CDCl3, 75.4 MHz) δ166.4, 145.6, 134.2, 130.5, 128.9, 128.2, 117.3, 64.1, 41.8.

Источник

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