反応式
[H-].[Na+].[CH3:3][N:4]([CH3:9])[CH2:5][CH2:6][CH2:7][OH:8].[CH2:10](Br)[CH:11]=[CH2:12]>CC(C)=O>[CH2:12]([O:8][CH2:7][CH2:6][CH2:5][N:4]([CH3:9])[CH3:3])[CH:11]=[CH2:10]参加物
反応条件
- 温度
- 0 °C
実験手順
Sodium hydride (17.5 g) and dimethyl formaldehyde (400 mL) were added to a 2-L round-bottom flask. After cooling the flask to 0° C. by immersing in an ice bath, 3-dimethylamino-1-propanol (0.398 mol) was added. After stirring for about 30 minutes and adding allyl bromide (0.4378 mol), the mixture was stirred for 3 hours after raising the temperature of the reactor to room temperature. Upon completion of reaction, the reaction was terminated by adding water to the flask and the product was extracted using diethyl ether. The extract was concentrated under reduced pressure and used in the next step without further purification. After filtration under reduced pressure, 3-(allyloxy)-N,N-dimethylpropan-1-amine was obtained through fractional distillation. Structural analysis was performed by NMR spectroscopy.
後処理
- customby immersing in an ice bath
- stirringthe mixture was stirred for 3 hours
- temperatureafter raising the temperature of the reactor to room temperature
- customUpon completion of reaction
- customthe reaction was terminated
- additionby adding water to the flask
- extractionthe product was extracted
- concentrationThe extract was concentrated under reduced pressure
- customused in the next step without further purification
- filtrationAfter filtration under reduced pressure
出典と根拠
- ORDレコード
- ord-18e2561901ff49ad83a89a70e1d2ff11
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434751B2
関連ノート
読み込み中…