Sodium Hydroxide → 4-Bromo-2,5-dimethylpyridine

HRID 879686Notes

Reaction equation

HRID 879686 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([N+]([O-])=O)[C:5]([CH3:11])=[CH:4][N+:3]=1[O-].P(Br)(Br)[Br:14].[OH-].[Na+]>CCOC(C)=O>[Br:14][C:6]1[C:5]([CH3:11])=[CH:4][N:3]=[C:2]([CH3:1])[CH:7]=1

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 24614Phosphorus tribromideHCID 146707Pyridine, 2,5-dimethyl-4-nitro-, 1-oxide

Product 1

HCID 223175304-Bromo-2,5-dimethylpyridine

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent2×

Procedure

Bromination. To a solution of 1.65 g of 2,5-dimethyl-4-nitro-pyridine 1-oxide in 50 mL dry EtOAc was added 11.1 mL PBr3 at rt. The mixture was heated to reflux over 0.5 h. Reflux continued for 3 h, then cooled to rt and poured into ice and EtOAc. The resulting mixture was brought to pH 10 with addition of NaOH pellets and layers were separated. An additional EtOAc extraction was combined with the first and the organic layers were washed with brine, dried whith Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (hexanes-EtOAc) to provide 4-bromo-2,5-dimethyl-pyridine (248 mg). LCMS (m/z) 186.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux over 0.5 h
  3. temperatureReflux
  4. customwere separated
  5. extractionAn additional EtOAc extraction
  6. washwere washed with brine
  7. dry with materialdried whith Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by column chromatography (hexanes-EtOAc)

Sources & evidence

ORD record
ord-64a0270b3c774aeaa55b250e733043e9
Source dataset
uspto-grants-2015_03
Patent number
US08987295B2

Reaction notes

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