Hydrogen Peroxide → 2-(Trifluoromethyl)pyridine 1-oxide
Reaktionsgleichung
[F:1][C:2]([F:10])([F:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1.[OH:11]O>C(O)(=O)C>[F:1][C:2]([F:10])([F:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N+:4]=1[O-:11]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
To a stirred solution of 2-trifluoromethyl pyridine (5 g, 34 mmol) in acetic acid (25 mL) is added 33% of aqueous H2O2 (20 mL) at room temperature. The reaction mixture is allowed to stir for 12 h at 70° C. After complete consumption of starting material the reaction mixture is concentrated under reduced pressure. The residue is dissolved in chloroform (250 mL) and pH is adjusted to 7 with K2CO3 (20 g approx). Resulting solid is filtered through glass sintered funnel and washed with chloroform. Filtrate is concentrated under reduced pressure to give 2-trifluoromethyl-pyridine 1-oxide as syrupy liquid (4.3 g).
Aufarbeitung
- customAfter complete consumption of starting material the reaction mixture
- concentrationis concentrated under reduced pressure
- dissolutionThe residue is dissolved in chloroform (250 mL)
- customResulting solid
- filtrationis filtered through glass sintered funnel
- washwashed with chloroform
- concentrationFiltrate is concentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-595de53777d74446aa43ab85662dfa98
- Quelldatensatz
- uspto-grants-2013_01
- Patentnummer
- US08362249B2
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