Hydrochloric Acid → (2S,3S)-3-(dibenzylamino)-2-hydroxyhexanoic acid
反応式
[CH2:1]([N:8]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C@@H:9]([CH2:14][CH2:15][CH3:16])[C@H](O)C#N)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[OH-:25].[Na+].[C:27]([O:30]CC)(=[O:29])[CH3:28].CCCCCC>>[CH2:17]([N:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C@@H:9]([CH2:14][CH2:15][CH3:16])[C@H:28]([OH:25])[C:27]([OH:30])=[O:29])[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1参加物
5
反応条件
- 温度
- 100 °C
実験手順
To (2S,3S)-3-(dibenzylamino)-2-hydroxyhexanenitrile (93.0 g; 0.301 mol) was added 12N hydrochloric acid (465 mL). The resulting mixture was heated to reflux (100° C.) for 3 hours, monitoring progress of the reaction by TLC analysis (ethyl acetate/hexane, 1:1). After TLC analysis indicated that the reaction was complete, the reaction mixture was cooled, and the pH was adjusted to 6-7 using 6N aqueous sodium hydroxide solution (930 mL). The product was extracted with two portions of dichloromethane (2×700 mL), and the combined organic phases were dried over sodium sulfate. After filtration the solvent was removed under reduced pressure, to give 95.0 g (96%) of (2S,3S)-3-(dibenzylamino)-2-hydroxyhexanoic acid as a solid.
後処理
- temperatureThe resulting mixture was heated
- temperaturethe reaction mixture was cooled
- extractionThe product was extracted with two portions of dichloromethane (2×700 mL)
- dry with materialthe combined organic phases were dried over sodium sulfate
- filtrationAfter filtration the solvent
- customwas removed under reduced pressure
出典と根拠
- ORDレコード
- ord-e9744ddf2c58440f99eb1c3780e489a6
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08431733B2
反応ノート
読み込み中…