Hydrogen Bromide → 2,5-Dibromo-4-propylpyridine
反応式
[Br:1][C:2]1[C:3]([CH2:9][CH2:10][CH3:11])=[CH:4][C:5](N)=[N:6][CH:7]=1.[BrH:12].BrBr.N([O-])=O.[Na+].[OH-].[Na+]>O>[Br:12][C:5]1[CH:4]=[C:3]([CH2:9][CH2:10][CH3:11])[C:2]([Br:1])=[CH:7][N:6]=1参加物
反応条件
- 温度
- -10 °C
実験手順
5-Bromo-4-propylpyridine-2-amine (5.67 g, 26.3 mmol) was added 48% hydrogen bromide (21 mL) at 10° C. The mixture was added bromine (4.0 mL) under ice-cold conditions, and added dropwise with an aqueous solution (4.5 mL) of sodium nitrite (4.54 g) at −10° C. The mixture was stirred at −10° C. for 0.5 hours, then added 1N aqueous solution of sodium hydroxide (10 mL), and stirred at room temperature for 2 hours. The reaction solution was added water, extracted with diethylether. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was purified by silica-gel column chromatography (diethylether), and the title compound (6.96 g (yield 95%)) was obtained as a brown oil.
後処理
- stirringstirred at room temperature for 2 hours
- extractionextracted with diethylether
- washThe organic layer was washed with brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
- customThe obtained residue was purified by silica-gel column chromatography (diethylether)
出典と根拠
- ORDレコード
- ord-7732ee161c1c418896b0526ffca541db
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08551985B2
反応ノート
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