Reaktionsgleichung
[ClH:1].[NH2:2][C@@H:3]([C:9]([OH:11])=[O:10])[CH2:4][CH2:5][CH2:6][CH2:7][NH2:8].C(O)C.CC(C)=O>C(O)(=O)C.C(=O)C1C(=CC=CC=1)O>[ClH:1].[NH2:2][CH:3]([C:9]([OH:11])=[O:10])[CH2:4][CH2:5][CH2:6][CH2:7][NH2:8]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
6 g of D-lysine monohydrochloride were dissolved in 180 ml of an aqueous 95% acetic acid solution, and 0.34 ml of salicylaldehyde was added thereto. The mixture was stirred at 100° C. for 3 hours. After the reaction, the mixture was condensed. 30 ml of 50% ethanol-acetone were added to the residue, and the crystalline precipitates were collected by filtration. 5.6 g of DL-lysine monohydrochloride were thereby obtained.
Aufarbeitung
- additionwas added
- customAfter the reaction
- customcondensed
- customthe crystalline precipitates
- filtrationwere collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-4f89e8343cde4b438e067a55fe787f2c
- Quelldatensatz
- uspto-grants-1983_08
- Patentnummer
- US04401820
Verknüpfte Notizen
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