Methyl iodide → 3-Bromo-2-methoxypyridine

HRID 1872521Notes

Reaction equation

HRID 1872521 reaction equation
[Br:1][C:2]1[C:3]([OH:8])=[N:4][CH:5]=[CH:6][CH:7]=1.I[CH3:10]>C1C=CC=CC=1.C(=O)([O-])[O-].[Ag+2]>[Br:1][C:2]1[C:3]([O:8][CH3:10])=[N:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Procedure

Under an argon atmosphere, a mixture of 3-bromo-2-hydroxypyridine (3.49 g, 20 mmol), silver carbonate (3.67 g, 13.31 mmol), and iodomethane (1.5 mL, 24.1 mmol) in benzene (30 mL) was stirred in the dark at 40° C. to 50° C. for 24 hours, cooled in an ice bath, and filtered. The filtrate was washed once with 2% aqueous sodium bicarbonate and twice with water, dried (MgSO4), the benzene was evaporated at atmospheric pressure, and the residue was purified by flash chromatography (eluting with hexane/ethyl acetate, 2:1) to obtain the title compound (2.35 g, 12.5 mmol, 62%).

Workup

  1. temperaturecooled in an ice bath
  2. filtrationfiltered
  3. washThe filtrate was washed once with 2% aqueous sodium bicarbonate and twice with water
  4. dry with materialdried (MgSO4)
  5. customthe benzene was evaporated at atmospheric pressure
  6. customthe residue was purified by flash chromatography (eluting with hexane/ethyl acetate, 2:1)

Sources & evidence

ORD record
ord-4be5407b16504421b51edba4eaac8ab9
Source dataset
uspto-grants-2000_08
Patent number
US06110914

Reaction notes

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