Dimethylamine → 2,4-Dichloro-6-(dimethylamino)-1,3,5-triazine
Reaktionsgleichung
[N:1]1[C:8]([Cl:9])=[N:7][C:5](Cl)=[N:4][C:2]=1[Cl:3].[CH3:10][NH:11][CH3:12]>CCOCC>[Cl:9][C:8]1[N:1]=[C:2]([Cl:3])[N:4]=[C:5]([N:11]([CH3:12])[CH3:10])[N:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
A suspension of cyanuric chloride (27.6 g.) in anhydrous ether (600 ml.) was kept at -30° C. and treated with dimethylamine (13.5 g.). Following the addition the mixture was allowed to warm to 0° C. and poured on to ice. The ether layer was separated, dried, kand evaporated and the residue crystallised from light petroleum to give the product (26.0 g.) having a melting point of 123°-124° C.
Aufarbeitung
- customwas kept at -30° C.
- additionthe addition the mixture
- additionpoured on to ice
- customThe ether layer was separated
- customdried
- customevaporated
- customthe residue crystallised from light petroleum
- customto give the product (26.0 g.)
Quellen und Nachweise
- ORD-Eintrag
- ord-268bf0d197194a8f95d104798829cfe2
- Quelldatensatz
- uspto-grants-1980_10
- Patentnummer
- US04226990
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