Reaktionsgleichung
[CH3:1][NH2:2].Cl.[N:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:10][CH2:11]Cl)[CH:5]=1.[OH-].[Na+].[Cl-].[Na+]>>[CH3:1][NH:2][CH2:11][CH2:10][C:6]1[CH:5]=[N:4][CH:9]=[CH:8][CH:7]=1Komponenten
5
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
To 32.6 g of 40% aqueous methylamine solution was added 7.48 g (0.042 mole) of 2-(3-pyridyl)ethyl chloride hydrochloride in small portions with stirring. The mixture was transfered to a stainless steel reaction column and heated at an external temperature of 80° C. for 4 hours. After cooling, 3.36 g of NaOH was added with ice-cooling and stirring and the mixture was saturated with sodium chloride and extracted with CH2Cl2. The extract was dried over MgSO4 and the CH2Cl2 was distilled off to give 6.32 g of the title compound in crude form as a yellow oil.
Aufarbeitung
- temperatureAfter cooling
- temperaturecooling
- stirringstirring
- extractionextracted with CH2Cl2
- dry with materialThe extract was dried over MgSO4
- distillationthe CH2Cl2 was distilled off
Quellen und Nachweise
- ORD-Eintrag
- ord-dbb7fe6b4f0c445f834aa9bd274f8366
- Quelldatensatz
- uspto-grants-1993_05
- Patentnummer
- US05214152
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