Reaktionsgleichung
[H-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH:8]=[CH:9][CH:10]=1)[NH2:7].[CH3:11][C:12]([CH3:17])=[CH:13][C:14](Cl)=[O:15]>C1COCC1>[CH3:11][C:12]([CH3:17])=[CH:13][C:14]([NH:7][C:6]1[CH:8]=[CH:9][CH:10]=[C:4]([Br:3])[CH:5]=1)=[O:15]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a suspension of NaH (4.15 g, 173 mmol, 60% in oil) in 50 ml of THF was cannulated a solution of 20.322 g (118 mmol) of 3-bromoaniline in 50 ml of THF. The resulting mixture was stirred at 0° C. for 45 min and warmed to room temperature over a period of 15 min. To this solution was added through cannulation 13.123 g (173 mmol) of 3,3-dimethylacryloyl chloride. The mixture was stirred at room temperature for 24 h and thereafter slowly poured into ice water. The resulting mixture was extracted with methylene chloride (twice), dried over MgSO4 and concentrated to yield a solid. The solid was purified by recrystallization in hexane/EtOAc (2:1) to give the title compound as a light brown solid.
Aufarbeitung
- temperaturewarmed to room temperature over a period of 15 min
- stirringThe mixture was stirred at room temperature for 24 h
- extractionThe resulting mixture was extracted with methylene chloride (twice),
- dry with materialdried over MgSO4
- concentrationconcentrated
- customto yield a solid
- customThe solid was purified by recrystallization in hexane/EtOAc (2:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-f8bece95ebe842d5ad74ccb6ba019094
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05616712
Verknüpfte Notizen
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