Acetic Anhydride → Diethyl[3-(acetylamino)propyl]phosphonate
反応式
[CH2:1]([O:3][P:4]([CH2:9][CH2:10][CH2:11][NH2:12])(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2].[C:13](OC(=O)C)(=[O:15])[CH3:14]>N1C=CC=CC=1>[CH2:6]([O:5][P:4]([CH2:9][CH2:10][CH2:11][NH:12][C:13](=[O:15])[CH3:14])(=[O:8])[O:3][CH2:1][CH3:2])[CH3:7]参加物
4
実験手順
97 g. of 3-aminopropanephosphonic acid diethyl ester is dissolved in 400 ml. of dry pyridine and 55 g. of acetic anhydride is added with stirring. The mixture is then boiled for 4 hours with refluxing and freed of the low-boiling components by evaporation in a light vacuum. Gaschromatographically pure N-acetyl-3-aminopropanephosphonic acid diethyl ester is obtained in a 96% yield by shortcut distillation in vacuo. It is a pale yellow, highly viscous oil with a boiling point of 166° to 160° C. (0.4 Torr).
後処理
- temperaturewith refluxing
- customfreed of the low-boiling components by evaporation in a light vacuum
出典と根拠
- ORDレコード
- ord-9844bdada756410ba5bfbd9cd3a8f9a3
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04029679
反応ノート
読み込み中…