Реакция #2467980

ord-fcff23db83a04a1b84c2510255576fcb

Уравнение реакции

O=S(=O)(O)O
Sulfuric acid
O=[N+]([O-])O
nitric acid
O=C(O)c1cccs1
thiophene-2-carboxylic acid
O=C(O)c1cc([N+](=O)[O-])cs1
product
Выход 75.0%
O=C(O)c1cc([N+](=O)[O-])cs1
4-Nitrothiophene-2-carboxylic acid
Выход 75.0%

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added to the above nitration mixture slowly for 15 min at the same temperature
  2. 2
    workup.ADDITIONThe reaction mixture was poured into ice cold water
  3. 3
    workup.STIRRINGstirred for 30 min
  4. 4
    ФильтрацияThe precipitated solid was filtered
  5. 5
    Промывкаwashed with cold water
  6. 6
    Другоеdried
  7. 7
    ЭкстракцияThe filtrate was extracted with ethyl acetate
  8. 8
    ПромывкаThe combined ethyl acetate layer was washed with water, brine
  9. 9
    Сушкаdried over sodium sulfate
  10. 10
    ФильтрацияThe solution was filtered
  11. 11
    Другоеevaporated the solvent
  12. 12
    workup.STIRRINGThe combined product was stirred with hexane (2×50 mL)
  13. 13
    Фильтрацияfiltered the solid
  14. 14
    Другоеdried

Методика

Sulfuric acid (3.0 mL, 5.505 g, 56.17 mmol) was added to nitric acid (2.0 mL, 2.98 g, 49.6 mmol) slowly at 0-10° C. After completion of the addition, thiophene-2-carboxylic acid (2.8 g, 21.87 mmol) was added to the above nitration mixture slowly for 15 min at the same temperature and stirred the mixture for 1 h. The reaction mixture was poured into ice cold water and stirred for 30 min. The precipitated solid was filtered, washed with cold water and dried. The filtrate was extracted with ethyl acetate. The combined ethyl acetate layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The combined product was stirred with hexane (2×50 mL) and filtered the solid and dried to give the product as an off-white solid (2.8 g, 75%), mp 110-118° C. The product was a mixture of two compounds by HPLC and 1H NMR and was proceeded to the next step.

Источник

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