反応式
[NH:1]1[CH2:16][CH2:15][CH2:14][CH2:13][CH:2]1[C:3]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4].C(=O)(O)[O-].[Na+]>C(OCC)(=O)C>[NH:1]1[CH2:16][CH2:15][CH2:14][CH2:13][C@H:2]1[C:3]([O:5][CH2:6][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1)=[O:4]参加物
4
実験手順
Benzyl pipecolate was routinely generated by treating an ethyl acetate suspension of this salt with saturated sodium bicarbonate until dissolution of the organic material. The aqueous layer was extracted twice with ethyl acetate and the combined organic extracts were dried with MgSO4 and evaporated to yield (S)-Benzyl pipecolate (15) as a pale yellow oil.
後処理
- additionby treating
- dissolutionuntil dissolution of the organic material
- extractionThe aqueous layer was extracted twice with ethyl acetate
- dry with materialthe combined organic extracts were dried with MgSO4
- customevaporated
出典と根拠
- ORDレコード
- ord-33e550e839574adb8a666652f05d88e9
- 出典データセット
- uspto-grants-1993_03
- 特許番号
- US05192773
関連ノート
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