Reaktionsgleichung
[CH3:1][N:2]1[CH:6]=[C:5]([CH3:7])[C:4]([C:8]([OH:10])=O)=[N:3]1.S(Cl)([Cl:13])=O>>[CH3:1][N:2]1[CH:6]=[C:5]([CH3:7])[C:4]([C:8]([Cl:13])=[O:10])=[N:3]1Komponenten
3
Versuchsvorschrift
1,4-Dimethyl-1H-pyrazole-3-carboxylic acid (190 mg) was weighed to a round bottom flask and thionyl chloride (1 ml) was added. The reaction was heated to reflux for 6 h then overnight at RT. After this time thionyl chloride was evaporated and the residue azeotroped with toluene to afford the title compound, 200 mg.
Aufarbeitung
- temperatureThe reaction was heated
- temperatureto reflux for 6 h
- customovernight
- customat RT
- customAfter this time thionyl chloride was evaporated
- customthe residue azeotroped with toluene
Quellen und Nachweise
- ORD-Eintrag
- ord-c376dc8ae7c445a988d94f474b950868
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09326987B2
Verknüpfte Notizen
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