反応式
C(NC(=O)O)C1C=CC=CC=1.[CH3:12][O:13][C:14]1([O:19][CH3:20])[CH2:18][CH2:17][NH:16][CH2:15]1.[H][H]>CO.[Pd]>[CH3:12][O:13][C:14]1([O:19][CH3:20])[CH2:18][CH2:17][NH:16][CH2:15]1参加物
5
実験手順
The 2.21 g of 3,3-dimethoxy-pyrrolidine benzyl carbamate, from step 3, dissolved in 100 mL of methanol, 2.21 g of Pd/C (wet) was added, and placed under 4 atm of hydrogen for 20 hours. The catalyst was filtered off using a 0.45 micro millipore filter and the solvent was evaporated to afford the title compound.
後処理
- filtrationThe catalyst was filtered off
- filtrationfilter
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-8db8cb3449b64d54a778053f320dfcbb
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05137892
関連ノート
読み込み中…