Hydrochloric Acid → HCID 86754565, Verbindung
Reaktionsgleichung
[NH2:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][SH:4].[CH2:8](O)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[ClH:19]>C(OCC)(=O)C>[ClH:19].[CH2:8]([O:6][C:5](=[O:7])[C@H:2]([CH2:3][SH:4])[NH2:1])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 150 °C
Versuchsvorschrift
L-Cysteine (157.4 g) was added to 250 ml of decyl alcohol saturated with dry HCl. The mixture was heated to 150° C. for 6 hours. The solution was cooled and was mixed with an equal volume of ethyl acetate. The solution was cooled in a dry ice bath to give crystals. The crystals were filtered and were then recrystallized from ethyl acetate, mp 96°-99° C., yield 100 g, IR (KBr) 1745 cm-1.
Aufarbeitung
- temperatureThe solution was cooled
- temperatureThe solution was cooled in a dry ice bath
- customto give crystals
- filtrationThe crystals were filtered
- customwere then recrystallized from ethyl acetate, mp 96°-99° C., yield 100 g, IR (KBr) 1745 cm-1
Quellen und Nachweise
- ORD-Eintrag
- ord-5441f168e1134cddb9a9c2a99401cd95
- Quelldatensatz
- uspto-grants-1981_05
- Patentnummer
- US04268441
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