Hydrochloric Acid → (2S)-3-(4-{2-[(4-Chlorobenzyl)(ethyl)amino]-2-oxoethoxy}phenyl)-2-ethoxypropanoic Acid
反応式
[Cl:1][C:2]1[CH:31]=[CH:30][C:5]([CH2:6][N:7]([CH2:28][CH3:29])[C:8](=[O:27])[CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([CH2:17][C@H:18]([O:24][CH2:25][CH3:26])[C:19]([O:21]CC)=[O:20])=[CH:13][CH:12]=2)=[CH:4][CH:3]=1.[Li+].[OH-].Cl>C1COCC1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]([CH2:28][CH3:29])[C:8](=[O:27])[CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([CH2:17][C@H:18]([O:24][CH2:25][CH3:26])[C:19]([OH:21])=[O:20])=[CH:13][CH:12]=2)=[CH:30][CH:31]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of ethyl(2S)-3-(4-{2-[(4-chlorobenzyl)(ethyl)amino]-2-oxoethoxy}phenyl)-2-ethoxypropanoate (0.240 g, 0.54 mmol) in THF (30 mL) was added aqueous 0.10 M LiOH (15 mL) and the solution was stirred at room temperature overnight. After neutralisation with 5% HCl, the solvent volume was reduced in vacuo and the remaining aqueous phase was acidified with 5% HCl and extracted with methylene chloride (2×50 mL). The combined organic phase was washed with brine (50 mL), dried over Na2SO4, and concentrated in vacuo. Purification on a prepacked column of silica gel (Isolute® SPE Column, 2 g/15 mL) with ethyl acetate as the eluent afforded 0.138 g (61%) of a pale yellow oil.
後処理
- extractionextracted with methylene chloride (2×50 mL)
- washThe combined organic phase was washed with brine (50 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customPurification on a prepacked column of silica gel (Isolute® SPE Column, 2 g/15 mL) with ethyl acetate as the eluent
出典と根拠
- ORDレコード
- ord-f857f7770d09479795b841b470cd350d
- 出典データセット
- uspto-grants-2009_02
- 特許番号
- US07488844B2
反応ノート
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