Hydrochloric Acid → 5-Chloro-6-methylpyridine-2-carbonitrile
Reaktionsgleichung
N[C:2]1[CH:3]=[CH:4][C:5]([C:9]#[N:10])=[N:6][C:7]=1[CH3:8].[ClH:11]>CC#N.Cl[Cu]>[Cl:11][C:2]1[CH:3]=[CH:4][C:5]([C:9]#[N:10])=[N:6][C:7]=1[CH3:8]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
A solution of 5-amino-6-methylpicolinonitrile (2) (260 mg, 1.95 mmol), CuCl (290 mg, 2.93 mmol) and t-BuONO (456 mg, 3.9 mmol) in CH3CN (10 mL) was stirred at room temperature under N2 for 2 h, and then warmed to 60° C. After 2 h, 10 mL 6N HCl was added and extracted with EA (3×10 mL). The organic phase was dried with anhydrous Na2SO4, filtered and concentrated. The residue was purified by Prep-TLC using PE/EtOAc=1/1 to give title compound as oil.
Aufarbeitung
- extractionextracted with EA (3×10 mL)
- dry with materialThe organic phase was dried with anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by Prep-TLC
Quellen und Nachweise
- ORD-Eintrag
- ord-9f23e741220f48faaf969e926c077df4
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09353104B2
Notizen zur Reaktion
Wird geladen…