Ethanol → Ethyl 2-chloroisonicotinate

HRID 1169675Notes

Reaction equation

HRID 1169675 reaction equation
S(=O)(=O)(O)O.[Cl:6][C:7]1[CH:12]=[C:11]([C:13]([OH:15])=[O:14])[CH:10]=[CH:9][N:8]=1.[CH2:16](O)[CH3:17]>O>[Cl:6][C:7]1[CH:12]=[C:11]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:10]=[CH:9][N:8]=1

Participants

5

Procedure

1 ml of concentrated sulfuric acid is added to a solution of 2.2 g of 2-chloropyridine-4-carboxylic acid in 30 ml of ethanol. The reaction mixture is refluxed with stirring for 16 hours and then concentrated to dryness under reduced pressure. The residue thus obtained is taken up in 30 ml of water and then extracted with 3×30 ml of dichloromethane. The organic phase is dried over magnesium sulfate, filtered and then concentrated to dryness under reduced pressure. The oil thus obtained is purified by filtration through 13 g of silica, eluting with dichloromethane. The fractions containing the expected product are concentrated to dryness under reduced pressure. 2.1 g of ethyl 2-chloropyridine-4-carboxylate are thus obtained.

Workup

  1. temperatureThe reaction mixture is refluxed
  2. concentrationconcentrated to dryness under reduced pressure
  3. customThe residue thus obtained
  4. extractionextracted with 3×30 ml of dichloromethane
  5. dry with materialThe organic phase is dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness under reduced pressure
  8. customThe oil thus obtained
  9. filtrationis purified by filtration through 13 g of silica
  10. washeluting with dichloromethane
  11. additionThe fractions containing the expected product
  12. concentrationare concentrated to dryness under reduced pressure

Sources & evidence

ORD record
ord-151f90203b0e47cea2443cf3d16a5dfe
Source dataset
uspto-grants-2010_11
Patent number
US07825115B2

Reaction notes

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