Hydrochloric Acid → (2RS, 3S)-3-amino-2-hydroxy-5-methylhexyl methyl ether hydrochloride
反応式
[CH3:1][O:2][CH2:3][CH:4]([OH:21])[C@@H:5]([NH:10]C(OCC1C=CC=CC=1)=O)[CH2:6][CH:7]([CH3:9])[CH3:8].[ClH:22]>CO.[Pd]>[ClH:22].[CH3:1][O:2][CH2:3][CH:4]([OH:21])[C@@H:5]([NH2:10])[CH2:6][CH:7]([CH3:9])[CH3:8]参加物
5
実験手順
To a solution of 94 mg of the ether compound obtained in 10 ml of methanol was added 0.16 ml of a 2N-hydrochloric acid, and the mixture was hydrogenated over 10 mg of a 10% palladium charcoal under hydrogen atmosphere. After filtration of the catalyst, the filtrate was evaporated under reduced pressure to obtain 54 mg of (2RS, 3S)-3-amino-2-hydroxy-5-methylhexyl methyl ether hydrochloride as a colorless viscous oil.
後処理
- filtrationAfter filtration of the catalyst
- customthe filtrate was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-c156175a9a7544e6b452522edbcaa4e9
- 出典データセット
- uspto-grants-1989_06
- 特許番号
- US04841067
反応ノート
読み込み中…