Реакция #2467967

ord-2ed853de447e46498067723a1a038e31

Уравнение реакции

COC(=O)c1cc(O)c(C(=O)OC)s1
Methyl 4-hydroxy-5-(methoxycarbonyl)thiophene-2-carboxylate
O=S(=O)(O)O
sulfuric acid
O=[N+]([O-])O
nitric acid
COC(=O)c1sc(C(=O)OC)c([N+](=O)[O-])c1O
semi-solid
Выход 20.0%
COC(=O)c1sc(C(=O)OC)c([N+](=O)[O-])c1O
Methyl 4-hydroxy-5-(methoxycarbonyl)-3-nitrothiophene-2-carboxylate
Выход 20.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONThe mixture was poured into ice
  2. 2
    Экстракцияextracted with ethyl acetate (3×100 mL)
  3. 3
    ПромывкаThe combined organic layer was washed with water, brine
  4. 4
    Сушкаdried over sodium sulfate
  5. 5
    ФильтрацияThe solution was filtered
  6. 6
    Другоеevaporated the solvent
  7. 7
    ДругоеThe 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%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08258119B2uspto-grants-2012_09