Nitric Acid → 3-chloro-1-Methyl-4-nitro-1H-pyrazole
Reaktionsgleichung
[Cl:1][C:2]1[CH:6]=[CH:5][N:4]([CH3:7])[N:3]=1.[N+:8]([O-])([OH:10])=[O:9]>S(=O)(=O)(O)O>[Cl:1][C:2]1[C:6]([N+:8]([O-:10])=[O:9])=[CH:5][N:4]([CH3:7])[N:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 3-chloro-1-methylpyrazole (Maybridge, Basel, Switzerland, 953 mg, 8.18 mmol) in concentrated sulfuric acid (1.4 ml), cooled with an ice-bath, was added over 30 min fuming nitric acid (1.19 mL, 28.6 mmol). The reaction mixture was stirred at rt for 2 h before being poured on ice/water and extracted with EtOAc (2×). The organic layers were washed with saturated aqueous NaHCO3 (2×) and brine, dried over Na2SO4, filtered, evaporated and dried over vacuum to give the title compound as a white solid (HPLC tR 2.24 min (Method A); M+H=162 MS-ES)
Aufarbeitung
- additionbefore being poured on ice/water
- extractionextracted with EtOAc (2×)
- washThe organic layers were washed with saturated aqueous NaHCO3 (2×) and brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated
- customdried over vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-892208aa09c144218022f13a11eccf54
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08476294B2
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