Hydrochloric Acid → 2-Chloro-3-iodo-4-methylpyridine
反応式
[Cl:1][C:2]1[C:7](N)=[C:6]([CH3:9])[CH:5]=[CH:4][N:3]=1.Cl.N([O-])=O.[Na+].[I-:15].[K+]>O>[Cl:1][C:2]1[C:7]([I:15])=[C:6]([CH3:9])[CH:5]=[CH:4][N:3]=1参加物
6
反応条件
- 温度
- 0 °C
実験手順
A mixture of 2-chloro-4-methylpyridin-3-amine (1.0 g, 7.0 mmol) and concentrated hydrochloric acid (4.4 mL) was cooled to 0° C. and a solution of sodium nitrite (0.5 g, 7.5 mmol) in water (8 mL) was added dropwise. The mixture was stirred for 1 hour at 0° C. and then was added dropwise to a stirred solution of potassium iodide (1.6 g, 9.6 mmol) in water (9 mL). The mixture was warmed to ambient temperature and stirred overnight. The mixture was extracted with diethyl ether and the organic phase was washed with aqueous sodium thiosulphate, brine, dried (MgSO4) and evaporated in vacuo. The crude product was recrystallized from hexane to give the title compound (0.88 g, 47%) as a white solid.
後処理
- temperatureThe mixture was warmed to ambient temperature
- stirringstirred overnight
- extractionThe mixture was extracted with diethyl ether
- washthe organic phase was washed with aqueous sodium thiosulphate, brine
- dry with materialdried (MgSO4)
- customevaporated in vacuo
- customThe crude product was recrystallized from hexane
出典と根拠
- ORDレコード
- ord-c52d24e593ba4ac082ea59c15fb19a41
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08450341B2
反応ノート
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