Реакция #46906

ord-0784ea4004a047fb97965e31f554cde6

Уравнение реакции

Oc1ccc(-c2cc(=S)ss2)cc1
5-p-hydroxyphenyl-1,2-dithiole-3-thione
CC(=O)Oc1ccccc1C(=O)O
acetylsalicylic acid
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
C(=NC1CCCCC1)=NC1CCCCC1
DCC
CC(=O)Oc1ccccc1C(=O)Oc1ccc(-c2cc(=S)ss2)cc1
4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-acetoxybenzoate
Выход 40.0%

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGstirred for 1 h at 0° C. and 3 h at room temperature
  2. 2
    ФильтрацияAfter filtration
  3. 3
    Другоеthe filtrate was evaporated under reduced pressure
  4. 4
    Другоеto remove the solvent
  5. 5
    ДругоеThe oily residue thus obtained
  6. 6
    Промывкаthe organic layer was washed with brine
  7. 7
    Сушкаdried on anhydrous MgSO4
  8. 8
    Фильтрацияfiltered
  9. 9
    Другоеthe solvent evaporated
  10. 10
    Промывкаeluted with ethyl ether/petroleum ether (1/1), from which 4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-acetoxybenzoate (3)
  11. 11
    Другоеwas obtained (354 mg, 40% yield)

Методика

To the solution of 1 (acetylsalicylic acid, 416 mg, 2.31 mmol) in 40 mL of dimethylformamide, hydroxybenzotriazole (343 mg, 2.54 mmol) and DCC (523 mg, 2.54 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 5-p-hydroxyphenyl-1,2-dithiole-3-thione (2; 574 mg, 2.54 mmol) was added and stirred for 1 h at 0° C. and 3 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product was loaded on a silica gel open column and eluted with ethyl ether/petroleum ether (1/1), from which 4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-acetoxybenzoate (3) was obtained (354 mg, 40% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07741359B2uspto-grants-2010_06