反応式
[CH2:1]1[CH:8]2[N:4]([C:5](=[O:9])[CH2:6][CH2:7]2)[C:3](=[O:10])[CH2:2]1.Cl.C.[OH2:13]>>[O:9]=[C:5]1[NH:4][CH:8]([CH2:1][CH2:2][C:3]([OH:10])=[O:13])[CH2:7][CH2:6]1参加物
5
反応条件
- 温度
- 100 °C
実験手順
A suspension (partial solution) of 25 g of dihydro-1H-pyrrolizine-3,5(2H,6H)-dione (III) in 150 ml of deionized water is treated with 0.1 ml of concentrated hydrochloric acid. The mixture is heated to reflux (100° C.) for 80 hours. Charcoal (0.5 g) is added and the mixture is filtered through filter aid. The solution is concentrated at reduced pressure, the 5-oxo-2-pyrrolidinepropanoic acid crystallizes and is isolated by filtration. After drying in vacuo the 5-oxo-2-pyrrolidinepropanoic acid has a melting point of 125°-127° C.
後処理
- temperatureThe mixture is heated
- filtrationthe mixture is filtered
- filtrationthrough filter aid
- concentrationThe solution is concentrated at reduced pressure
- customthe 5-oxo-2-pyrrolidinepropanoic acid crystallizes
- customis isolated by filtration
- dry with materialAfter drying in vacuo the 5-oxo-2-pyrrolidinepropanoic acid
出典と根拠
- ORDレコード
- ord-1985c5ec1c484e6487f633dd4706d4e7
- 出典データセット
- uspto-grants-1985_12
- 特許番号
- US04559358
関連ノート
読み込み中…