Methanol → Methyl 3-bromoisonicotinate Hydrochloride

HRID 31393Notes

Reaction equation

HRID 31393 reaction equation
Cl.[Br:2][C:3]1[CH:11]=[N:10][CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=[O:6].S(Cl)([Cl:14])=O.[CH3:16]O>C(OCC)(=O)C.CN(C=O)C>[ClH:14].[Br:2][C:3]1[CH:11]=[N:10][CH:9]=[CH:8][C:4]=1[C:5]([O:7][CH3:16])=[O:6]

Participants

6

Procedure

To a stirred suspension of 3-bromoisonicotinic acid hydrochloride (27.4 g, 0.10 mol) in ethyl acetate (250 ml) was added one drop of DMF followed by thionyl chloride (18.5 g, 0.16 mol). The mixture was heated at reflux for 1 h and allowed to cool to room temperature. The mixture was then concentrated under reduced pressure to give an off-white solid. To this was added methanol and this was refluxed for 2 hrs. The mixture was then concentrated under reduced pressure and diluted with ethyl acetate. The precipitate was collected on filter paper on a Buchner funnel. The white solid was washed with ethyl acetate and air-dried. The white solid was placed in a vacuum oven at 60° C. overnight with a nitrogen bleed. Yield: 18.5 g (71% th).

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 1 h
  3. concentrationThe mixture was then concentrated under reduced pressure
  4. customto give an off-white solid
  5. temperaturethis was refluxed for 2 hrs
  6. concentrationThe mixture was then concentrated under reduced pressure
  7. additiondiluted with ethyl acetate
  8. customThe precipitate was collected
  9. filtrationon filter paper on a Buchner funnel
  10. washThe white solid was washed with ethyl acetate
  11. customair-dried

Sources & evidence

ORD record
ord-12017e20021f467a8b28a740c514cdfb
Source dataset
uspto-grants-2008_09
Patent number
US07425639B2

Reaction notes

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