Trifluoroacetic acid → HCID 23149183, Verbindung

HRID 1983054Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1983054
[Cl:1][C:2]([Cl:19])([F:18])[S:3][C:4]1[CH:5]=[N:6][N:7](CC2C=CC(OC)=CC=2)[CH:8]=1.FC(F)(F)C(O)=O.C(=O)([O-])O.[Na+]>>[Cl:1][C:2]([Cl:19])([F:18])[S:3][C:4]1[CH:5]=[N:6][NH:7][CH:8]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

1.04 g of 4-{[dichlorofluoromethyl]thio}-1-(4-methoxybenzyl)-1H-pyrazole was dissolved to 6 ml of trifluoroacetic acid, followed by stirring at 65° C. for 3 hours. After the reaction mixture was cooled to room temperature, it was added to saturated aqueous solution of sodium hydrogen carbonate. The mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.19 g of 4-{[dichlorofluoromethyl]thio}-1H-pyrazole.

Aufarbeitung

  1. temperatureAfter the reaction mixture was cooled to room temperature
  2. extractionThe mixture was extracted with ethyl acetate
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-131e44626a8d4a1390e459e58d5a8591
Quelldatensatz
uspto-grants-2009_06
Patentnummer
US07541374B2

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