Acetonitrile → HCID 583430、化合物
反応式
[C:1](#[N:3])[CH3:2].C([Li])CCC.Br[C:10]1[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][N:11]=1>C1COCC1>[CH3:16][C:13]1[CH:14]=[CH:15][C:10]([CH2:2][C:1]#[N:3])=[N:11][CH:12]=1参加物
反応条件
- 温度
- 78 °C
実験手順
To a solution of anhydrous acetonitrile (10.1 mL, 191.83 mmol, 3.3 equiv.) in dry THF (500 mL) was added dropwise n-butyl lithium (2.5 M in hexane, 69.8 mL, 174.39 mmol, 3 equiv.) at minus 78° C. under a nitrogen atmosphere. The resulting white suspension was stirred at minus 78° C. for 1 hour, and then a solution of 2-bromo-5-methylpyridine (10.0 g, 58.13 mmol, 1 equiv.) in dry THF (30 mL) was added. The reaction mixture was kept at minus 78° C. for 1 hour and then warmed up slowly to room temperature and stirred for another hour. Ice/water was added and the layer was separated. The organic layer was washed with water and brine, dried over MgSO4, filtered, and evaporated to give 18 g of crude product, which was used for next step reaction without further purification.
後処理
- waitThe reaction mixture was kept at minus 78° C. for 1 hour
- temperaturewarmed up slowly to room temperature
- stirringstirred for another hour
- customthe layer was separated
- washThe organic layer was washed with water and brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated
出典と根拠
- ORDレコード
- ord-6f390e37b14a4008b2a673f8b0fed084
- 出典データセット
- uspto-grants-2015_07
- 特許番号
- US09072313B2
反応ノート
読み込み中…