Acetyl chloride → N-(Octan-2-yl)acetamide
反応式
[C:1](Cl)(=[O:3])[CH3:2].[CH3:5][CH:6]([NH2:13])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C(N(CC)CC)C>C1COCC1.C(OCC)(=O)C>[CH3:5][CH:6]([NH:13][C:1](=[O:3])[CH3:2])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]参加物
6
実験手順
A solution of acetyl chloride (7.11 mL, 100 mmol) was added dropwise to an ice water-cooled solution of 1-methylheptyl amine (8.30 g, 64 mmol) and triethylamine (20.91 mL, 150 mmol) in THF (100 mL). The resulting mixture was stirred at RT for 1 h, then was diluted with ethyl acetate and washed twice with 10% HCl, twice with sat aq NaHCO3, and then twice with brine. The organic solution was dried (MgSO4), and concentrated to afford 8.13 g N-(1-methylhept-1-yl)acetamide, a 73% yield.
後処理
- washwashed twice with 10% HCl, twice with sat aq NaHCO3
- dry with materialThe organic solution was dried (MgSO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-a1cf46430aac40bcab03f0e5f9c509e5
- 出典データセット
- uspto-grants-2000_02
- 特許番号
- US06028101
反応ノート
読み込み中…