反応式
C(O)(=O)[C@H]([C@@H](C(O)=O)O)O.[NH:11]1[CH2:16][CH2:15][CH2:14][C@H:13]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:12]1.[OH-].[Na+]>>[NH:11]1[CH2:16][CH2:15][CH2:14][C@H:13]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:12]1参加物
3
実験手順
To 13.0 g of ethyl (3S)-3-piperidinecarboxylate D(−)-tartarate which was synthesized following the method of P. Magnus, et al. [J. Org. Chem. Vol. 56, 1166-1170 (1991)], 3N aqueous sodium hydroxide solution was added to render the former basic, followed by extraction with chloroform and drying over anhydrous magnesium sulfate. Distilling the solvent off under reduced pressure, 7.50 g of the title compound was obtained.
後処理
- extractionfollowed by extraction with chloroform
- dry with materialdrying over anhydrous magnesium sulfate
- distillationDistilling the solvent off under reduced pressure
出典と根拠
- ORDレコード
- ord-96b0cc3b998343d5bc036a7bcedf6292
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07452908B2
関連ノート
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