Реакция #6482

ord-324cff6c10c54f0e868e67759e4a7ad4

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe layers were separated
  2. 2
    Экстракцияthe aqueous layer was extracted with methylene chloride
  3. 3
    ЭкстракцияThe combined organic extract
  4. 4
    Промывкаwas washed with 1N aqueous sodium hydroxide solution and brine
  5. 5
    Сушкаdried over anhydrous magnesium sulfate
  6. 6
    Фильтрацияfiltered
  7. 7
    workup.DISTILLATIONthe filtrate was distilled

Методика

To a solution of 33.9 g (280 mmol) of phenylacetaldehyde and 35.6 g (330 mmol) of 1,3-propanedithiol in 300 mL of methylene chloride at 0° C., was added, dropwise over a period of 30 minutes, 10 mL of boron trifluoride etherate. The reaction mixture was allowed to warm to ambient temperature and stirred for 3 h at ambient temperature. The reaction mixture was made basic by the addition of 180 mL of 5% aqueous potassium hydroxide solution and the resultant mixture was stirred for 0.5 h. The layers were separated and the aqueous layer was extracted with methylene chloride. The combined organic extract was washed with 1N aqueous sodium hydroxide solution and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate was distilled to afford 53.62 g (91% yield) of the title compound, b.p. 150° C. (2 mm Hg); 1H NMR (CDCl3) δ1.75-1.95 (1H, m), 2.05-2.17 (1H, m), 2.75-2.91 (4H, m), 3.03 (2H, d, J=9 Hz), 4.25 (1H, t, J=9 Hz), 7.17-7.38 (5H, m).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05248677uspto-grants-1993_09