反応式
[CH3:1][N:2]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH3:3].[Br:10][CH2:11][CH2:12][CH2:13][Cl:14]>CO>[Br-:10].[Cl:14][CH2:13][CH2:12][CH2:11][N+:2]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])([CH3:3])[CH3:1]参加物
4
反応条件
- 温度
- 65 °C
実験手順
A 500 mL, 3-necked, round-bottomed flask equipped with air condensers and a magnetic stirring plate was charged with N,N-dimethylhexylamine (199.46 grams, 1.54 moles), 1-bromo-3-chloropropane (243.00 grams, 1.54 moles) and 250 mL of methanol. The reaction was maintained at 65° C. for 24 hours. Solvent was removed by rotary evaporation under reduced pressure to yield a brown, viscous oil. Yield 445.8 grams (1.55 moles, 100%).
後処理
- customA 500 mL, 3-necked, round-bottomed flask equipped with air condensers
- customSolvent was removed by rotary evaporation under reduced pressure
- customto yield a brown, viscous oil
出典と根拠
- ORDレコード
- ord-041ae228686d4fae866668dc87ba5254
- 出典データセット
- uspto-grants-1999_10
- 特許番号
- US05969090
関連ノート
読み込み中…