Hydrochloric Acid → 2-Chloro-6-ethyl-3-(3-methylbenzoyl)pyridine
反応式
Br[C:2]1[CH:3]=[C:4]([CH3:8])[CH:5]=[CH:6][CH:7]=1.[Mg].[Cl:10][C:11]1[C:16]([C:17]#N)=[CH:15][CH:14]=[C:13]([CH2:19][CH3:20])[N:12]=1.[Cl-].[NH4+].Cl.[O:24]1CCCC1>>[Cl:10][C:11]1[C:16]([C:17](=[O:24])[C:6]2[CH:7]=[CH:2][CH:3]=[C:4]([CH3:8])[CH:5]=2)=[CH:15][CH:14]=[C:13]([CH2:19][CH3:20])[N:12]=1参加物
反応条件
- 温度
- -20 °C
実験手順
3-Bromotoluene (12.5 g, 73.1 mmol) was added to a tetrahydrofuran (200 ml) solution of magnesium (1.70 g, 70.0 mmol), and the mixture was stirred until magnesium pieces disappeared. The reaction solution was cooled to -20° C., mixed with 2-chloro-3-cyano-6-ethylpyridine (10.6 g, 63.6 mmol) and then stirred for 17 hours at room temperature. The reaction solution was mixed with saturated ammonium chloride aqueous solution and 1 N hydrochloric acid, and the mixture was stirred for 2 hours at room temperature and then extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was removed by filtration and then the filtrate was concentrated under a reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 2-chloro-6-ethyl-3-(3-methylbenzoyl)pyridine (9.19 g, 56%) as a yellow oily material.
後処理
- stirringthe mixture was stirred for 2 hours at room temperature
- extractionextracted with ethyl acetate
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate
- customwas removed by filtration
- concentrationthe filtrate was concentrated under a reduced pressure
- customThereafter, the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate)
出典と根拠
- ORDレコード
- ord-f28148fc2cb842f4be863bdff7b7f5c5
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06136810
反応ノート
読み込み中…