Reaktionsgleichung
C(OC([NH:8][C@@H:9]([CH3:15])[CH2:10][O:11][N+:12]([O-:14])=[O:13])=O)(C)(C)C.CCOCC.[ClH:21].O1CCOCC1>>[ClH:21].[CH3:15][C@H:9]([NH2:8])[CH2:10][O:11][N+:12]([O-:14])=[O:13]Komponenten
4
Versuchsvorschrift
In 80 ml of 4N hydrochloric acid-dioxane were dissolved 4.52 g of (1S)-N-(t-butoxycarbonyl)-1-methyl-2-nitroxyethylamine, and the mixture was left to stand at room temperature for 1 hour and 50 minutes. To the mixture were added 160 ml of ether, and the crystals were collected by filtration and dried to obtain 3.02 g of the desired compound as colorless crystals.
Aufarbeitung
- waitthe mixture was left
- filtrationthe crystals were collected by filtration
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-21634171d01d4347a88d48f984cf1d4f
- Quelldatensatz
- uspto-grants-1999_04
- Patentnummer
- US05891898
Verknüpfte Notizen
Wird geladen…