反応式
[C:1]([O:4][C:5]1[CH:27]=[CH:26][CH:25]=[CH:24][C:6]=1[C:7]([O:9][CH2:10][CH2:11][CH2:12][NH:13]C(OCC1C=CC=CC=1)=O)=[O:8])(=[O:3])[CH3:2]>[Pd].CO>[C:1]([O:4][C:5]1[CH:27]=[CH:26][CH:25]=[CH:24][C:6]=1[C:7]([O:9][CH2:10][CH2:11][CH2:12][NH2:13])=[O:8])(=[O:3])[CH3:2]参加物
4
実験手順
A mixture of 3-(benzyloxycarbonylamino)propyl 2-acetoxybenzoate (2.0 g, 5.4 mmol), 10% Pd/C (0.2 g) and CH3OH (50 mL) was stirred under a H2 atmosphere (RT, 16 h). The mixture was filtered and concentrated under reduced pressure to afford a colorless oil. Purification by silica chromatography afforded 3-aminopropyl 2-acetoxybenzoate as a colorless oil. Mass calculated for C12H15NO4=237.25. found: [M+H]+=238.3.
後処理
- filtrationThe mixture was filtered
- concentrationconcentrated under reduced pressure
- customto afford a colorless oil
- customPurification by silica chromatography
出典と根拠
- ORDレコード
- ord-c7ab94aa62a44fe3be378d32964d111c
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08729293B2
関連ノート
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