Реакция #2467965

ord-6fca64d3a1884b18955fbf65c9878219

Уравнение реакции

[NH4+].[OH-]
ammonium hydroxide
COC(=O)c1sccc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
O=S(=O)(O)O
sulfuric acid
O=[N+]([O-])O
nitric acid
COC(=O)c1sc([N+](=O)[O-])cc1N=NN(C)C
solid
Выход 26.0%
COC(=O)c1sc([N+](=O)[O-])cc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylate
Выход 26.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONThe mixture was poured into ice
  2. 2
    ЭкстракцияThe solution was extracted with chloroform (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 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate (2 g, 9.38 mmol) was added slowly for 15 min at 0 to −5° C. to concentrated sulfuric acid (20 mL). Then concentrated nitric acid (0.54 mL, 70%, 10.7 mmol) was added to the above reaction mixture for 10 min and stirred at the same temperature for 1 h and rt for 16 h. The mixture was poured into ice cooled water and basified with ammonium hydroxide. The solution was extracted with chloroform (3×100 mL) and 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 hexane-ethyl acetate (80:20) as eluents to give the product as a yellow color solid (450 mg, 26%), mp 128-130° C.

Источник

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