Hydrochloric Acid → 4-nitro- DL-Phenylalanine, methyl ester, monohydrochloride
Reaktionsgleichung
[N+:1]([C:4]1[CH:15]=[CH:14][C:7]([CH2:8][C@@H:9]([C:11]([OH:13])=[O:12])[NH2:10])=[CH:6][CH:5]=1)([O-:3])=[O:2].[ClH:16].[CH3:17]O>>[ClH:16].[NH2:10][CH:9]([CH2:8][C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:15][CH:14]=1)[C:11]([O:13][CH3:17])=[O:12]Komponenten
4
Versuchsvorschrift
A solution of p-nitro-L-phenylalanine (12.6 g) and c.HCl (7.5 g) in methanol (150 ml) was refluxed for 1.5 hours and the solvent then evaporated in vacuo. The residue was triturated with ether and recrystallised from SVM to give the desired product as a off-white solid, [α]25 +15.3° (c=0.55, MeOH).
Aufarbeitung
- customthe solvent then evaporated in vacuo
- customThe residue was triturated with ether
- customrecrystallised from SVM
Quellen und Nachweise
- ORD-Eintrag
- ord-71a8162ecd834347b161bb44eb91ad7d
- Quelldatensatz
- uspto-grants-1993_07
- Patentnummer
- US05225431
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