Thionyl Chloride → HCID 22938786, Verbindung
Reaktionsgleichung
[CH2:1]([N:3]1[CH:7]=[N:6][N:5]=[C:4]1[CH2:8]O)[CH3:2].S(Cl)([Cl:12])=O>>[ClH:12].[Cl:12][CH2:8][C:4]1[N:3]([CH2:1][CH3:2])[CH:7]=[N:6][N:5]=1Komponenten
3
Versuchsvorschrift
To 4-ethyl-3-hydroxymethyl-4H-1,2,4-triazole (4.6 g), thionyl chloride (36 ml) was slowly added at 0° C. The mixture was heated to reflux for 1 hour, and concentrated under reduced pressure. To the residue was added ethyl acetate and ethanol, and the precipitated crystals were collected by filtration. The crystals were washed with ethyl acetate, to give 3-chloromethyl-4-ethyl-4H-1,2,4-triazole hydrochloride (4.22 g) as orange crystals.
Aufarbeitung
- temperatureThe mixture was heated
- temperatureto reflux for 1 hour
- concentrationconcentrated under reduced pressure
- additionTo the residue was added ethyl acetate and ethanol
- filtrationthe precipitated crystals were collected by filtration
- washThe crystals were washed with ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-72fe571441664a4e9be409866d900805
- Quelldatensatz
- uspto-grants-2007_08
- Patentnummer
- US07262185B2
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