C[O:2][C:3]1[C:4]([C:9]2[CH:10]=[C:11]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:13][CH:14]=2)=[N:5][CH:6]=[CH:7][CH:8]=1.[BrH:18]>>[BrH:18].[OH:2][C:3]1[C:4]([C:9]2[CH:10]=[C:11]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:13][CH:14]=2)=[N:5][CH:6]=[CH:7][CH:8]=1A solution of 3-(3-methoxypyridin-2-yl)nitrobenzene (0.5 g) in 47% hydrobromic acid (10 ml) was stirred at 130° C. for 24 hours. After cooling, the precipitate was collected by filtration, washed with water and acetone and dried to give 3-(3-hydroxypyridin-2-yl)-nitrobenzene hydrobromide (0.54 g).
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