Hydrogen Bromide → 5-(Bromomethyl)-2-o-tolylpyridine hydrobromide
反応式
[C:1]1([CH3:15])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[N:12]=[CH:11][C:10]([CH2:13]O)=[CH:9][CH:8]=1.[BrH:16]>>[BrH:16].[Br:16][CH2:13][C:10]1[CH:9]=[CH:8][C:7]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[CH3:15])=[N:12][CH:11]=1参加物
3
実験手順
A solution of 4.49 g (22.5 mmol) of (6-o-tolylpyridin-3-yl)methanol in 75 mL of 48% hydrobromic acid was heated to reflux for 64 h. The reaction mixture was partially cooled and excess hydrobromic acid was removed by vacuum distillation (110° C. @ 2 Torr) until a tan solid residue remained in the flask. Distillation was carried out using a large KOH pellet trap placed between the distillation apparatus and the vacuum pump. The solid residue was slurried in diethyl ether, filtered and dried under a nitrogen stream to give 7.38 g of product, 95% yield.
後処理
- temperatureto reflux for 64 h
- temperatureThe reaction mixture was partially cooled
- customexcess hydrobromic acid was removed by vacuum distillation (110° C. @ 2 Torr) until a tan solid residue