Hydrogen Sulfide → 5-Hydroxynicotinic acid

HRID 1011446

Reaktionsgleichung

Reaktionsgleichung von HRID 1011446
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].S.[OH2:12]>[Cu]>[OH:12][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8]

Komponenten

5

Versuchsvorschrift

To 10.1 g (0.05 mol) of 5-bromonicotinic acid was added 10 g of NaOh dissolved in 63 mL of water, 3.1 g of coppersulfate pentahydrate and 0.42 g of copper (0). The reaction mixture was vigorously stirred and heated under reflux for 30 hours. After cooling the mixture to room temperature, 4.8 g of Na2S.H2O was added and stirring was pursued overnight. The reaction mixture was heated to 70° C. and treated with H2S gas until disappearance of the white precipitate (3 h). After cooling to room temperature, the mixture was filtered and the pH of the filtrate was adjusted to 5.2 with concentrated hydrochloric acid. The precipitate was filtered and the pH of the % filtrate was adjusted to 4.6 with concentrated hydrochloric acid. The white precipitate was then filtered, washed with water and dried under reduced pressure giving 4.3 g (yield: 62%) of product of molecular formula C7H5NO3. Aspect: white powder.

Aufarbeitung

  1. temperatureheated
  2. temperatureunder reflux for 30 hours
  3. stirringstirring
  4. temperatureThe reaction mixture was heated to 70° C.
  5. temperatureAfter cooling to room temperature
  6. filtrationthe mixture was filtered
  7. filtrationThe precipitate was filtered
  8. filtrationThe white precipitate was then filtered
  9. washwashed with water
  10. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-39e605143a2f487da16c435c9525b943
Quelldatensatz
uspto-grants-2011_07
Patentnummer
US07977354B2

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