Hydrochloric Acid → Methyl O-tert-butyl-L-tyrosinate hydrochloride
Reaktionsgleichung
[NH:1](C(OCC1C=CC=CC=1)=O)[C@H:2]([C:15]([O:17][CH3:18])=[O:16])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[CH:6][CH:5]=1.[ClH:29]>CO.[Pd].[O-]S([O-])(=O)=O.[Ba+2]>[NH2:1][C@H:2]([C:15]([O:17][CH3:18])=[O:16])[CH2:3][C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]([CH3:14])([CH3:12])[CH3:13])=[CH:8][CH:9]=1.[ClH:29]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
300 g (778 mmoles) of Z-Tyr(But)-OMe (Ann. Chem. 696, 226 (1966)) are dissolved in 1 liter of methanol and hydrogenated catalytically (Pd/BaSO4 catalyst) at pH 4.5, using an auto-burette (about 2 N methanolic HCl being added). After completion of hydrogenation, the catalyst is filtered off and the filtrate is concentrated. The residue is triturated with ether.
Aufarbeitung
- filtrationAfter completion of hydrogenation, the catalyst is filtered off
- concentrationthe filtrate is concentrated
- customThe residue is triturated with ether
Quellen und Nachweise
- ORD-Eintrag
- ord-1056f3f79e874fd4a3a7c1eba6adf64f
- Quelldatensatz
- uspto-grants-1980_07
- Patentnummer
- US04212796
Notizen zur Reaktion
Wird geladen…