Dimethylformamide → HCID 178434610, Verbindung
Reaktionsgleichung
[CH3:1][C:2]1[CH:6]=[C:5]([C:7]([F:10])([F:9])[F:8])[NH:4][N:3]=1.CN(C=O)C.[Cl:16]N1C(=O)CCC1=O>O>[Cl:16][C:6]1[C:2]([CH3:1])=[N:3][NH:4][C:5]=1[C:7]([F:10])([F:9])[F:8]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
3-methyl-5-trifluoromethylpyrazole was taken into dry DMF (20 mL) and N-chloro succinimide (1.78 g) was added in portions. The mixture was then heated at 70° C. for 22 h, cooled to room temperature, and then water (100 mL) was added and the mixture extracted with ethyl acetate (4×25 mL). The organic layer was washed with water and brine and dried with Na2SO4. Evaporation of the solvent afforded the title compound.
Aufarbeitung
- additionwas added in portions
- temperaturecooled to room temperature
- extractionthe mixture extracted with ethyl acetate (4×25 mL)
- washThe organic layer was washed with water and brine
- dry with materialdried with Na2SO4
- customEvaporation of the solvent
Quellen und Nachweise
- ORD-Eintrag
- ord-54f8eead3ef64bd1b4ef90c1484c3d55
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07449576B1
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