benzyl 2(S)-morpholinocarbonyloxy-3-phenylpropionate → O-(N-Morpholinocarbonyl)-3-phenyllactic acid
反応式
[O:1]1[CH2:6][CH2:5][N:4]([C:7]([O:9][C@@H:10]([CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:11]([O:13]CC2C=CC=CC=2)=[O:12])=[O:8])[CH2:3][CH2:2]1.[H][H]>CO.[Pd]>[O:1]1[CH2:6][CH2:5][N:4]([C:7]([O:9][C@@H:10]([CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:11]([OH:13])=[O:12])=[O:8])[CH2:3][CH2:2]1参加物
5
実験手順
A solution of benzyl 2(S)-morpholinocarbonyloxy-3-phenylpropionate (300 mg) in methanol (20 ml) was hydrogenated over 10% palladium on carbon (30 mg) at 3 atmospheric pressure of hydrogen for 1 hour. The solution was filtered and concentrated in vacuo to give 2(S)-morpholinocarbonyloxy-3-phenylpropionic acid (220 mg) as an oil.
後処理
- filtrationThe solution was filtered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-31828a16a6974f39b08103f9625d5911
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05223489
反応ノート
読み込み中…