3,5-Difluorothiophenol → 5-(3,5-Difluorophenylthio)furan-3-carboxylic Acid

HRID 894248Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 894248
[F:1][C:2]1[CH:3]=[C:4]([SH:9])[CH:5]=[C:6]([F:8])[CH:7]=1.Br[C:11]1[O:15][CH:14]=[C:13]([C:16]([OH:18])=[O:17])[CH:12]=1>CN(C)C=O>[F:1][C:2]1[CH:3]=[C:4]([S:9][C:11]2[O:15][CH:14]=[C:13]([C:16]([OH:18])=[O:17])[CH:12]=2)[CH:5]=[C:6]([F:8])[CH:7]=1

Komponenten

4

Edukt 2

HCID 27583613,5-DifluorothiophenolHCID 133335605-Bromofuran-3-carboxylic acid

Produkt 1

HCID 211624485-(3,5-Difluorophenylthio)furan-3-carboxylic Acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

In an open flask, cuprous oxide (0.6 g., 4 mmoles) and 3,5-difluorothiophenol (0.76 g., 4 mmoles) were combined with 25 ml. of dimethylformamide and heated in an oil bath maintained at 150°-160° C. for 2 hours. 5-Bromofuran-3-carboxylic acid was added, the flask was equipped with a reflux condenser, and heating at 150°-155° C. was continued for 16 hours. The reaction mixture was cooled, filtered, the filtrate diluted with 150 ml. of water and product extracted into two 30 ml. portions of ethyl acetate. The combined ethyl acetate extracts were back-washed with water, evaporated to an oil, the oil taken up in ether, product extracted into 12 ml. of 1 N sodium hydroxide, the basic extract acidified with conc. hydrochloric acid and the product extracted back into fresh ether and evaporated to yield crude product as an oil. The oil was chromatographed on approximately 100 ml. of silica gel with hexane/5% acetic acid as eluant, clean fractions (Rf 0.2 on thin layer chromatography with the same eluant) were combined, concentrated to dryness, and crystallized by trituration with hexane to yield purified 5-(3,5-difluorophenylthio)furan-3-carboxylic acid (127 mg., m.p. 128°-130° C., m/e 256).

Aufarbeitung

  1. temperaturemaintained at 150°-160° C. for 2 hours
  2. customthe flask was equipped with a reflux condenser
  3. temperatureheating at 150°-155° C.
  4. temperatureThe reaction mixture was cooled
  5. filtrationfiltered
  6. additionthe filtrate diluted with 150 ml
  7. extractionof water and product extracted into two 30 ml
  8. washThe combined ethyl acetate extracts were back-washed with water
  9. customevaporated to an oil
  10. extractionproduct extracted into 12 ml
  11. extractionof 1 N sodium hydroxide, the basic extract
  12. extractionthe product extracted back into fresh ether
  13. customevaporated
  14. customto yield crude product as an oil
  15. customThe oil was chromatographed on approximately 100 ml
  16. concentrationconcentrated to dryness
  17. customcrystallized by trituration with hexane
  18. customto yield
  19. custompurified 5-(3,5-difluorophenylthio)furan-3-carboxylic acid (127 mg., m.p. 128°-130° C., m/e 256)

Quellen und Nachweise

ORD-Eintrag
ord-7a7f2bea11e04bf392c976a29a98234f
Quelldatensatz
uspto-grants-1981_08
Patentnummer
US04282246

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