Reaktion #2467980

ord-fcff23db83a04a1b84c2510255576fcb

Reaktionsgleichung

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
Ausbeute 75.0%
O=C(O)c1cc([N+](=O)[O-])cs1
4-Nitrothiophene-2-carboxylic acid
Ausbeute 75.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  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
    FiltrationThe precipitated solid was filtered
  5. 5
    Waschenwashed with cold water
  6. 6
    Sonstigedried
  7. 7
    ExtraktionThe filtrate was extracted with ethyl acetate
  8. 8
    WaschenThe combined ethyl acetate layer was washed with water, brine
  9. 9
    Trocknendried over sodium sulfate
  10. 10
    FiltrationThe solution was filtered
  11. 11
    Sonstigeevaporated the solvent
  12. 12
    workup.STIRRINGThe combined product was stirred with hexane (2×50 mL)
  13. 13
    Filtrationfiltered the solid
  14. 14
    Sonstigedried

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08258119B2uspto-grants-2012_09