Reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:8])=[N:6][CH:7]=1.[Br:9]Br.O>N1C=CC=CC=1>[Br:9][C:7]1[C:2]([OH:1])=[CH:3][CH:4]=[C:5]([CH3:8])[N:6]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 5-hydroxy-2-methylpyridine (Commercial, Aldrich, 44.5 g) in pyridine (400 ml) is added dropwise over 30 min at room temperature a solution of bromine (71.64 g) in pyridine (550 ml). The reaction mixture was stirred for an additional 1.5 h. The reaction mixture was poured into water (4 liters), stirred for a few minutes and extracted with diethyl ether (4×300 ml). The combined organics were dried over sodium sulphate and concentrated in vacuo to give a brown solid that was purified through silica using a 0-30% ethyl acetate in hexane system, to give the title compound as a beige solid, 37 g.
Workup
- stirringstirred for a few minutes
- extractionextracted with diethyl ether (4×300 ml)
- dry with materialThe combined organics were dried over sodium sulphate
- concentrationconcentrated in vacuo
- customto give a brown solid that
- customwas purified through silica using a 0-30% ethyl acetate in hexane system
Sources & evidence
- ORD record
- ord-de1f22ae142f40d19354d3e3e9e166b7
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08993560B2
Linked notes
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