Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[N:6][C:5]([CH3:8])=[CH:4][N:3]=1.Cl.[CH3:10][NH:11][CH3:12].[CH2:13]=O.[OH-].[Na+]>O>[CH3:10][N:11]([CH3:13])[CH2:12][CH2:1][C:2]1[CH:7]=[N:6][C:5]([CH3:8])=[CH:4][N:3]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 140 °C
Versuchsvorschrift
A mixture of 75.0 g (0.7 mole) of 2,5-dimethylpyrazine and 41.0 g (0.5 mole) of dimethylamine hydrochloride was heated at 140° C. 60.0 g (38% aqueous solution) (0.75 mole) of formaldehyde was added over a period of two hours. After two hours additional heating the mixture was cooled. It was diluted with 110 ml of water, made basic with 10% sodium hydroxide and extracted with chloroform. The solvent was removed and the residue distilled to give 28.6 g of 2-(β-dimethylaminoethyl)-5-methylpyrazine, b.p. 106°-110° C. at 10 mm Hg.
Aufarbeitung
- temperatureAfter two hours additional heating the mixture
- temperaturewas cooled
- extractionextracted with chloroform
- customThe solvent was removed
- distillationthe residue distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-8e7c5d9d62e44642ad0dfac211e1259f
- Quelldatensatz
- uspto-grants-1980_01
- Patentnummer
- US04183933
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