反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][NH2:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].ClC(Cl)(Cl)[CH:16](O)[OH:17].C(Cl)(Cl)Cl>O>[CH:16]([NH:13][CH2:12][CH2:11][C:5]1[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=1)=[O:17]参加物
5
反応条件
- 温度
- 120 °C
実験手順
First, 2-(3,4-dimethoxyphenyl)-ethylamine (181.2 g, 1 mol) and chloral hydrate (181 g, 1.1 mol) are mixed together and heated to 120° C., with stirring, for 20 minutes and any volatile components (chloroform and water) are eliminated in a water jet vacuum at an oil bath temperature of 140° C. An oil is left behind which is further processed without any purification.
後処理
- customtemperature of 140° C
- waitAn oil is left behind which
- customis further processed without any purification
出典と根拠
- ORDレコード
- ord-e687a79b375e40ad8ca7776ad80c5a88
- 出典データセット
- uspto-grants-1987_07
- 特許番号
- US04678792
関連ノート
読み込み中…