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Sodium Iodide → 6-Iodopyridine-3-carboxylic acid

HRID 53379
Notes
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Reaction equation

HRID 53379 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 5238Sodium IodideHCID 24841Hydrogen iodideHCID 792226-Chloronicotinic acid

Product 1

HCID 8190626-Iodopyridine-3-carboxylic acid

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

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.

Workup

  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)

Sources & evidence

ORD record
ord-b6665b274db740d495d2125d751f579c
Source dataset
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05618931

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes