Reaktionsgleichung
S(Cl)([Cl:3])=O.[NH2:5][C@@H:6]([C:14]([OH:16])=[O:15])[CH2:7][CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.Cl.[CH3:18]O>>[NH2:5][C@@H:6]([C:14]([O:16][CH3:18])=[O:15])[CH2:7][CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.[ClH:3]Komponenten
4
Versuchsvorschrift
To cold (-20° C.) and dry methanol (195 ml) was added dropwise thionylchloride (28 ml). H-D-Cha-OH.HCl (40 g) was added and the reaction mixture was heated under reflux for 5 h. The mixture was concentrated in vacuo and coevaporated with methanol (3 times). The residue was crystallized from methanol/diethylether yielding H-D-Cha-OMe.HCl as a crystalline powder (40.9 g).
Aufarbeitung
- temperaturethe reaction mixture was heated
- temperatureunder reflux for 5 h
- concentrationThe mixture was concentrated in vacuo
- customThe residue was crystallized from methanol/diethylether
Quellen und Nachweise
- ORD-Eintrag
- ord-c2b9a4d80e344b6a9e13ee2c99e330f1
- Quelldatensatz
- uspto-grants-2000_03
- Patentnummer
- US06034067
Verknüpfte Notizen
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