[F:1][C:2]1[CH:11]=[CH:10][C:9]([O:12]C)=[CH:8][C:3]=1[CH2:4][N:5]([CH3:7])[CH3:6].[BrH:14].C(O)(=O)C>>[BrH:14].[CH3:7][N:5]([CH2:4][C:3]1[CH:8]=[C:9]([OH:12])[CH:10]=[CH:11][C:2]=1[F:1])[CH3:6](2-Fluoro-5-methoxybenzyl)-dimethylamine (1.51 g, 8.24 mmol) was heated to reflux in 30% hydrogen bromide/acetic acid (10 mL) for 17 h. The cooled reaction mixture was triturated and decanted with successive portions of diethyl ether (4×), then triturated with diethyl ether overnight. The solid was collected by filtration, washed with ether and dried to give 3-dimethylaminomethyl-4-fluorophenol hydrobromide (1.43 g, 69%) as a tan solid.
読み込み中…