L-Aspartic acid diethyl ester hydrochloride → 1,4-Dimethyl L-aspartate
反応式
Cl.[CH2:2]([O:4][C:5](=[O:14])[C@H:6]([CH2:8][C:9]([O:11][CH2:12]C)=[O:10])[NH2:7])C>C(=O)([O-])[O-].[Na+].[Na+]>[NH2:7][C@H:6]([C:5]([O:4][CH3:2])=[O:14])[CH2:8][C:9]([O:11][CH3:12])=[O:10]参加物
3
実験手順
Diethylaspartate hydrochloride (3, 85.31 g, 0.432 mol) was dissolved in a saturated solution of aqueous sodium carbonate (200 mL) and extracted with ethyl acetate (10×250 mL) in a separatory funnel. The combined organic phases were dried by filtration through magnesium sulfate and sodium sulfate and concentrated in vacuo to provide dimethyl aspartate (58.73 g, 0.364 mol, 84%) as a pale yellow oil. This material provided satisfactory 1H NMR data and was used immediately in the preparation of N-benzyloxycarbonylglycyl-L-α-aspartic acid dimethyl ester (5).
後処理
- extractionextracted with ethyl acetate (10×250 mL) in a separatory funnel
- dry with materialThe combined organic phases were dried by filtration through magnesium sulfate and sodium sulfate
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-a0f6b6fcd7e244e89c1dbf6460731807
- 出典データセット
- uspto-grants-1992_09
- 特許番号
- US05144073
反応ノート
読み込み中…