Reaktionsgleichung
C(OC(=O)[NH:7][CH2:8][CH2:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=1)(C)(C)C.[ClH:19]>O1CCOCC1>[ClH:19].[F:17][C:14]1[CH:15]=[CH:16][C:11]([O:10][CH2:9][CH2:8][NH2:7])=[CH:12][CH:13]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
Next, to a solution of [2-(4-fluorophenoxy)ethyl]carbamic acid tert-butyl ester (7.0 g, 27.4 mmol) in dioxane (20 mL) cooled in an ice bath was added 4N—HCl in dioxane (100 mL) dropwise. The mixture was stirred at 0° C. for 2 hours, and at room temperature for 16 hours. The precipitates were filtered, washed with diethylether, and dried under reduced pressure to yield 2-(4-fluorophenoxy)ethylamine HCl salt (4.24 g, 80.7% yield).
Aufarbeitung
- waitat room temperature for 16 hours
- filtrationThe precipitates were filtered
- washwashed with diethylether
- customdried under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-54903767278b4fbbaa8fd42caec3bb42
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07423175B2
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