Dimethylformamide → N-(4-formyl-3,5-dimethyl-phenyl)-acetamide
反応式
Br[C:2]1[C:7]([CH3:8])=[CH:6][C:5]([NH:9][C:10](=[O:12])[CH3:11])=[CH:4][C:3]=1[CH3:13].[Li]CCCC.CN([CH:22]=[O:23])C>C1COCC1>[CH:22]([C:2]1[C:7]([CH3:8])=[CH:6][C:5]([NH:9][C:10](=[O:12])[CH3:11])=[CH:4][C:3]=1[CH3:13])=[O:23]参加物
5
反応条件
- 温度
- -78 °C
実験手順
To a solution of N-(4-bromo-3,5-dimethyl-phenyl)-acetamide (150 mg) in THF (5 mL) was added n-BuLi (1.36 mL, 1.0 M solution in hexane) at −78° C. The mixture was stirred at −78° C. for 30 min, then warmed up to −40° C. for 5 min, then cooled down to at −78° C. again. After 20 min, DMF (0.24 mL) was added. The mixture was stirred at −78° C. for 30 min and then allowed to warm up to room temperature for 1 h. The reaction was quenched with saturated NH4Cl aqueous solution and extracted with EtOAc. The organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give N-(4-formyl-3,5-dimethyl-phenyl)-acetamide: MS (m/z) 192 (M+1).
後処理
- temperaturewarmed up to −40° C. for 5 min
- temperaturecooled down to at −78° C. again
- waitAfter 20 min
- stirringThe mixture was stirred at −78° C. for 30 min
- temperatureto warm up to room temperature for 1 h
- customThe reaction was quenched with saturated NH4Cl aqueous solution
- extractionextracted with EtOAc
- washThe organic extracts were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-54ca4c150d3345b795c0bcc0dad7c55d
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08222248B2
反応ノート
読み込み中…