Isopropyl iodide → HCID 22493581, compound

HRID 2269239Notes

Reaction equation

HRID 2269239 reaction equation
[C:1](=O)([O-])[O-].[K+].[K+].I[CH:8]([CH3:10])[CH3:9].C([O:14][CH2:15][CH3:16])(=O)C.CCCCCC.[Cl:23][C:24]1[C:25](O)=[N:26][CH:27]=[C:28]([CH:32]=1)[C:29]([OH:31])=[O:30]>>[Cl:23][C:24]1[CH:25]=[N:26][CH2:27][C:28]([O:14][CH:15]([CH3:16])[CH3:1])([C:29]([O:31][CH:8]([CH3:10])[CH3:9])=[O:30])[CH:32]=1

Participants

5

Reactant 4

HCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 21226206Ethyl acetate hexaneHCID 178524771HCID 178524771, compound

Product 1

HCID 22493581HCID 22493581, compound

Conditions

Temperature
8 °C

Procedure

In 20 ml of N,N-diimethylformamide were dissolved 1.0 g of 5-chloro-6-hydroxynicotinic acid. To the resulting solution were added 4.78 g of potassium carbonate and 1.26 ml of 2-iodopropane, followed by stirring under heat at 8° C. for 4 hours. Ice water was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The organic layer was successively washed with water and saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column (developing solvent: 5% ethyl acetate/n-hexane), whereby 600 mg of the title compound were obtained.

Workup

  1. extractionthe resulting mixture was extracted with ethyl acetate
  2. washThe organic layer was successively washed with water and saturated saline
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue so obtained

Sources & evidence

ORD record
ord-9fb2998643a14eff9d1eae3d2a772f94
Source dataset
uspto-grants-2001_12
Patent number
US06329402B1

Reaction notes

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