Реакция #46906
ord-0784ea4004a047fb97965e31f554cde6
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGstirred for 1 h at 0° C. and 3 h at room temperature
- 2ФильтрацияAfter filtration
- 3Другоеthe filtrate was evaporated under reduced pressure
- 4Другоеto remove the solvent
- 5ДругоеThe oily residue thus obtained
- 6Промывкаthe organic layer was washed with brine
- 7Сушкаdried on anhydrous MgSO4
- 8Фильтрацияfiltered
- 9Другоеthe solvent evaporated
- 10Промывкаeluted with ethyl ether/petroleum ether (1/1), from which 4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-acetoxybenzoate (3)
- 11Другоеwas 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).