Hydrochloric Acid → 1-(Benzyloxycarbonylamino)-2-phenylethyl-phosphonic acid
Reaktionsgleichung
[CH2:1]([O:8][C:9]([NH:11][CH:12]([P:20]([OH:22])[OH:21])[CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].[O-:25][Mn](=O)(=O)=O.[K+].P(O)O.Cl.S(=O)(O)[O-].[Na+]>CC(C)=O.O>[CH2:1]([O:8][C:9]([NH:11][CH:12]([P:20](=[O:25])([OH:21])[OH:22])[CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Komponenten
9
Edukt 6
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of 1-benzyloxycarbonylamino2-phenylethyl phosphonous acid (0.5 g, 0.0016 mole) in acetone (20 ml) and water (10 ml) was added a 10% solution of sodium hydroxide in water until a pH of about 7 was reached. A solution of KMnO4 (0.14 g, 0.00086 mole, 0.55 equiv.) in water (10 ml) was added slowly to the vigorously stirred solution of phosphonous acid at 20-25° C. After the addition (5 minutes), the reaction mixture was stirred for 5 minutes at ambient temperature and acidified with concentrated HCl acid until a pH of 1 was reached. Saturated sodium bisulfite solution was added to the reaction mixture thereby resulting in formation of a white precipitate.
Aufarbeitung
- additionAfter the addition (5 minutes)
- customthereby resulting in formation of a white precipitate
Quellen und Nachweise
- ORD-Eintrag
- ord-da1de098c3ae402db57b5e38d1d3a25a
- Quelldatensatz
- uspto-grants-1987_06
- Patentnummer
- US04670193
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