Reaktionsgleichung
[S:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[C:7]([CH2:10][CH2:11][O:12][CH2:13][CH2:14][CH2:15][N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH:8]=[CH:9][C:2]1=2.[C:21]([OH:26])(=[O:25])[C:22]([OH:24])=[O:23]>C(OCC)(=O)C>[C:21]([OH:26])(=[O:25])[C:22]([OH:24])=[O:23].[S:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[C:7]([CH2:10][CH2:11][O:12][CH2:13][CH2:14][CH2:15][N:16]([CH2:17][CH3:18])[CH2:19][CH3:20])[CH:8]=[CH:9][C:2]1=2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In 2 mL of ethyl acetate is dissolved 0.46 g of N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine, to which is added 2.5 mL of a solution of 0.15 g of oxalic acid in ethyl acetate. The resulting mixture is stirred at ambient temperature for 2 hours. The deposited crystal is collected by filtration, washed with ethyl acetate and dried to obtain 0.47 g of N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine oxalate.
Aufarbeitung
- filtrationThe deposited crystal is collected by filtration
- washwashed with ethyl acetate
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-1f0ea39af0b748bab5f24a13e5e63a32
- Quelldatensatz
- uspto-grants-2004_09
- Patentnummer
- US06797726B1
Verknüpfte Notizen
Wird geladen…