تفاعل #6482

ord-324cff6c10c54f0e868e67759e4a7ad4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe layers were separated
  2. 2
    استخلاصthe aqueous layer was extracted with methylene chloride
  3. 3
    استخلاصThe combined organic extract
  4. 4
    غسيلwas washed with 1N aqueous sodium hydroxide solution and brine
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    workup.DISTILLATIONthe filtrate was distilled

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248677uspto-grants-1993_09