Triethylamine → N-cycloheptyl-N-methylamine
反応式
[C:1]1(=O)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.CN.[CH2:12]([N:14](CC)CC)C>ClCCCl>[CH3:12][NH:14][CH:1]1[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1参加物
5
実験手順
In 1,2-dichloroethane (50 ml) were suspended cyclo-heptanone (2 g), methylamine hydrochloride (3 g) and triethylamine (6.2 ml), and to the suspension was added sodium triacetoxy boron hydride (5.3 g) under ice-cooling. Under nitrogen atmosphere, the mixture was stirred at room temperature over night. The solvent was evaporated, and the residue was neutralized with sodium hydroxide. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated to give N-methylcycloheptylamine (1.8 g) as colorless oil.
後処理
- temperaturecooling
- customThe solvent was evaporated
- extractionThe mixture was extracted with ethyl acetate
- washThe organic layer was washed with saturated sodium chloride solution
- dry with materialdried with anhydrous magnesium sulfate
- customUnder reduced pressure, the solvent was evaporated
出典と根拠
- ORDレコード
- ord-66add22207e5487ebf571719aa946b99
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06166006
反応ノート
読み込み中…