Reaktionsgleichung
[F:1][C:2]1[CH:22]=[CH:21][C:5]([O:6][CH2:7][CH2:8][O:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][NH2:18])=[CH:12][C:11]=2[O:19][CH3:20])=[CH:4][CH:3]=1.[ClH:23]>C(OCC)C>[ClH:23].[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][CH2:8][O:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][NH2:18])=[CH:12][C:11]=2[O:19][CH3:20])=[CH:21][CH:22]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 2-{4-[2-(4-fluoro-phenoxy)-ethoxy]-3-methoxy-phenyl}-ethylamine (15.7 g) dissolved in diethylether (200 ml) is added 1M hydrogen chloride solution in diethylether (75 ml). The resulting residue is isolated by separation in a centrifuge and decantation. 2-{4-[2-(4-Fluoro-phenoxy)-ethoxy]-3-methoxy-phenyl}-ethylamine hydrochloride is obtained.
Aufarbeitung
- customThe resulting residue is isolated by separation in a centrifuge and decantation
Quellen und Nachweise
- ORD-Eintrag
- ord-99ff543ae35a4990937d41086295e352
- Quelldatensatz
- uspto-grants-2003_03
- Patentnummer
- US06538016B2
Verknüpfte Notizen
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