Sodium Sulfite → 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfonylpyrazole
Reaktionsgleichung
ClC1C=CC=C(C(OO)=[O:9])C=1.ClC1C=C(C(F)(F)F)C=C(Cl)C=1C1C=C(SC)N(C)N=1.[Cl:32][C:33]1[CH:38]=[C:37]([C:39]([F:42])([F:41])[F:40])[CH:36]=[C:35]([Cl:43])[C:34]=1[C:44]1[CH:48]=[C:47]([S:49]([CH3:51])=[O:50])[N:46]([CH3:52])[N:45]=1.S([O-])([O-])=O.[Na+].[Na+]>C(Cl)(Cl)Cl>[Cl:43][C:35]1[CH:36]=[C:37]([C:39]([F:42])([F:40])[F:41])[CH:38]=[C:33]([Cl:32])[C:34]=1[C:44]1[CH:48]=[C:47]([S:49]([CH3:51])(=[O:9])=[O:50])[N:46]([CH3:52])[N:45]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 0.3 g quantity of 70% m-chloroperbenzoic acid was slowly added to 0.2 g of 3-(2,6-dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazole (compound 6) in 20 ml of anhydrous chloroform at room temperature with stirring, followed by further stirring overnight. The reaction mixture was poured into a 10% aqueous sodium sulfite solution, an organic layer was then separated off, washed with 5% aqueous sodium hydroxide solution and with brine and dried over anhydrous magnesium sulfate. The solvent was thereafter distilled off under reduced pressure, giving 0.3 g of the desired compound in the form of white crystals (quantitative crude yield).
Aufarbeitung
- stirringby further stirring overnight
- customan organic layer was then separated off
- washwashed with 5% aqueous sodium hydroxide solution and with brine
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe solvent was thereafter distilled off under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-98a0b3bab57c4faf8f1f3a06795f6f04
- Quelldatensatz
- uspto-grants-1998_04
- Patentnummer
- US05739083
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