反応式
CN(C)CCO.C([Li])CCC.[C:12]1([C:18]2[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(Br)(Br)(Br)[Br:25]>CCCCCC.O>[Br:25][C:22]1[CH:23]=[C:18]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:19]=[CH:20][N:21]=1参加物
反応条件
- 温度
- 0 °C
実験手順
To a solution of 2-dimethylaminoethanol (5.60 g, 62.8 mmol) in hexane (80 ml) was added dropwise 1.6N hexane solution of n-butyl lithium (78.5 ml, 125 mmol) under ice-cooling, and stirred at 0° C. for 30 minutes. Then, 4-phenylpyridine (3.24 g, 20.8 mmol) was added thereto, and stirred at 0° C. for 1 hour. After cooling the reaction solution to −78° C., a solution of carbon tetrabromide (25.0 g, 75.4 mmol) in hexane (40 ml) was added thereto, and stirred at −78° C. for 1 hour, then at room temperature for 1 hour. To the reaction solution was added water under ice-cooling, and extracted with ether. The extract was dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduce pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the titled compound 2.21 g (45.4%) as solid product.
後処理
- temperaturecooling
- stirringstirred at 0° C. for 1 hour
- temperatureAfter cooling the reaction solution to −78° C.
- stirringstirred at −78° C. for 1 hour
- waitat room temperature for 1 hour
- temperaturecooling
- extractionextracted with ether
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- distillationthe solvent was distilled away
- customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1)
出典と根拠
- ORDレコード
- ord-9d562519b434426ca73f9acfdde51242
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07812025B2
関連ノート
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