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Sodium Iodide → 6-Iodopyridine-3-carboxylic acid

HRID 1224
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1224
[I-:1].[Na+].I.Cl[C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][N:6]=1>CC(C)=O>[I:1][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][N:6]=1
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Komponenten

5

Edukt 3

HCID 5238Sodium IodideHCID 24841Hydrogen iodideHCID 792226-Chloronicotinic acid

Produkt 1

HCID 8190626-Iodopyridine-3-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

To 27.97 g (186.6 mmol) of sodium iodide cooled to -78° C. was added 121.77 g (71.6 ml, 952.0 mmol) of hydriodic acid (57 wt %). The reaction mixture was allowed to warm slightly with stirring for 5 minutes, and then 30.00 g (190.4 mmol) of 6-chloronicotinic acid was added. The resulting mixture was allowed to warm to room temperature with stirring and then heated at 120°-125° C. in an oil bath for 42 hours. A dark brown layer formed above the yellow solid material. The reaction mixture was allowed to cool to room temperature and then poured into acetone (chilled to 0° C.). The resultant yellow solid was collected by filtration, washed with 200 ml of 1N NaHSO3 solution, and dried in high vacuum (3 mm Hg) to give the title compound as a pale yellow solid.

Aufarbeitung

  1. temperatureto warm slightly
  2. stirringwith stirring
  3. temperatureheated at 120°-125° C. in an oil bath for 42 hours
  4. customA dark brown layer formed above the yellow solid material
  5. temperatureto cool to room temperature
  6. filtrationThe resultant yellow solid was collected by filtration
  7. washwashed with 200 ml of 1N NaHSO3 solution
  8. customdried in high vacuum (3 mm Hg)

Quellen und Nachweise

ORD-Eintrag
ord-9bd2bc35b4cb41778d4b4e86c4962f24
Quelldatensatz
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05723620

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