Ethanol → (2RS,3S)-3-(Benzyloxycarbonyl)amino-4-phenyl-1,2-butanediol
反応式
C(O)C.[Br-].[Li+].[CH2:6]([O:13][C:14]([NH:16][C@@H:17]([CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH:18]([OH:25])[C:19](OC(C)C)=[O:20])=[O:15])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[BH4-].[Na+]>O1CCCC1.O>[CH2:6]([O:13][C:14]([NH:16][C@@H:17]([CH2:26][C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)[CH:18]([OH:25])[CH2:19][OH:20])=[O:15])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1参加物
実験手順
Ethanol (1 ml) and lithium bromide (36.7 mg) are added to a solution of isopropyl (2RS,3S)-3-(benzyloxycarbonyl)amino-2-hydroxy-4-phenylbutyrate (150 mg, Reference compound No. 13-1) in tetrahydrofuran (1 ml). The mixture is cooled with ice, sodium borohydride (42.1 mg) is added to the mixture, and the temperature is raised to room temperature. The whole is stirred overnight, water is added thereto, and the whole is further stirred for one hour. The reaction mixture is concentrated under reduced pressure, and the resulting residue is extracted with ethyl acetate. The extract is washed with saturated brine and dried over anhydrous magnesium sulfate. The extract is concentrated under reduced pressure to give the titled reference compound (105 mg).
後処理
- additionis added to the mixture
- stirringthe whole is further stirred for one hour
- concentrationThe reaction mixture is concentrated under reduced pressure
- extractionthe resulting residue is extracted with ethyl acetate
- washThe extract is washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationThe extract is concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-8aad0e06e2514dcc847015f7deb1eda7
- 出典データセット
- uspto-grants-2005_11
- 特許番号
- US06960575B2
反応ノート
読み込み中…