Реакция #2467967
ord-2ed853de447e46498067723a1a038e31
Уравнение реакции
Methyl 4-hydroxy-5-(methoxycarbonyl)thiophene-2-carboxylate
sulfuric acid
nitric acid
→
semi-solid
Выход 20.0%
Methyl 4-hydroxy-5-(methoxycarbonyl)-3-nitrothiophene-2-carboxylate
Выход 20.0%
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1workup.ADDITIONThe mixture was poured into ice
- 2Экстракцияextracted with ethyl acetate (3×100 mL)
- 3ПромывкаThe combined organic layer was washed with water, brine
- 4Сушкаdried over sodium sulfate
- 5ФильтрацияThe solution was filtered
- 6Другоеevaporated the solvent
- 7ДругоеThe residue was chromatographed over silica gel column
Методика
Methyl 4-hydroxy-5-(methoxycarbonyl)thiophene-2-carboxylate (5 g, 23.14 mmol) was added slowly for 15 min at 0 to −5° C. to concentrated sulfuric acid (25 mL). Then concentrated nitric acid (3.2 mL, 70%, 34.7 mmol) was added to the above reaction mixture for 10 min and stirred at the same temperature for 1 h. The mixture was poured into ice cooled water and extracted with ethyl acetate (3×100 mL). The combined organic layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using chloroform-methanol (95:5) as eluents to give the product as a yellow color semi-solid (1.2 g, 20%).