Methyl iodide → 3-Bromo-2-methoxypyridine
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]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
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
- temperaturecooled in an ice bath
- filtrationfiltered
- washThe filtrate was washed once with 2% aqueous sodium bicarbonate and twice with water
- dry with materialdried (MgSO4)
- customthe benzene was evaporated at atmospheric pressure
- customthe residue was purified by flash chromatography (eluting with hexane/ethyl acetate, 2:1)
Sources & evidence
- ORD record
- ord-8491b1544a2849a8b98bcf685ae424b5
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06703502B2
Reaction notes
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