Hydrochloric Acid → (R)-N-Benzyl-2-acetamido-3-hydroxypropionamide
Reaktionsgleichung
[CH2:1]([NH:8][C:9](=[O:21])[C@@H:10]([CH2:15][O:16]C(C)(C)C)[NH:11][C:12](=[O:14])[CH3:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>ClCCl>[CH2:1]([NH:8][C:9](=[O:21])[C@@H:10]([CH2:15][OH:16])[NH:11][C:12](=[O:14])[CH3:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of N-benzyl-O-tert-butyl-N2-acetyl-D-serinamide (0.5 g) and dichloromethane (10 mL), aq. HCl 35% (5 mL) was added. The solution was stirred for 2 hours at room temperature for completion of reaction and after workup and crystallization gave solid 0.21 g N-benzyl-N2-acetyl-D-serinamide.
Aufarbeitung
- customafter workup and crystallization
Quellen und Nachweise
- ORD-Eintrag
- ord-a0f1aa6c5e884c97af6c6e32f3378777
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09242926B2
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