Sodium Hydroxide → 1-[3-(4-Bromobenzoyl)propionyl]-L-proline
反応式
C[O:2][C:3](=[O:22])[C@@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[C:9](=[O:21])[CH2:10][CH2:11][C:12](=[O:20])[C:13]1[CH:18]=[CH:17][C:16]([Br:19])=[CH:15][CH:14]=1.[OH-].[Na+]>>[Br:19][C:16]1[CH:17]=[CH:18][C:13]([C:12]([CH2:11][CH2:10][C:9]([N:5]2[CH2:6][CH2:7][CH2:8][C@H:4]2[C:3]([OH:22])=[O:2])=[O:21])=[O:20])=[CH:14][CH:15]=1参加物
3
実験手順
A mixture of 2.64 g. of 1-[3-(4-bromobenzoyl)propionyl]-L-proline methyl ester (Example 26) and 26 ml. of 1 N sodium hydroxide is stirred at room temperature. The solids are collected by decantation, dissolved in tetrahydrofuran and returned to the alkaline solution which is stirred further at room temperature. This alkaline solution is washed with ethyl acetate and poured into iced hydrochloric acid. This mixture is extracted with dichloromethane. The organic extract is dried over magnesium sulfate and evacuated to dryness in vacuo leaving a gum. This gum is triturated with ether giving white crystals which are recrystallized from acetone-hexane giving the desired product as 1.35 g. of white crystals, mp. 138°-139° C.
後処理
- additionA mixture of 2.64 g
- customThe solids are collected by decantation
- dissolutiondissolved in tetrahydrofuran
- washThis alkaline solution is washed with ethyl acetate
- additionpoured into iced hydrochloric acid
- extractionThis mixture is extracted with dichloromethane
- extractionThe organic extract
- dry with materialis dried over magnesium sulfate
- customevacuated to dryness in vacuo
- customleaving a gum
- customThis gum is triturated with ether giving white crystals which
- customare recrystallized from acetone-hexane giving the desired product as 1.35 g
出典と根拠
- ORDレコード
- ord-3b60a7f4d5dd4e778589b36f500403ac
- 出典データセット
- uspto-grants-1980_10
- 特許番号
- US04226775
反応ノート
読み込み中…