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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70254Erstellt: 24. Oktober 2026

Salicylaldehyde oxime → 1-(3-methyl-4-chlorophenyl)-3-(3-chlorophenyl)-1H-pyrazole

https://huagongshe.com/de/reaction/70254

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicylaldehyde oximeHCID 7200—
EduktCesium carbonateHCID 10796—
Edukt5-Bromo-2-chlorotolueneHCID 609899—
EduktHCID 178478050HCID 178478050—
KatalysatorCopper oxideHCID 14829—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(3-methyl-4-chlorophenyl)-3-(3-chlorophenyl)-1H-pyrazoleHCID 6678719021,7%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of 3-(3-chlorophenyl)-1H-pyrazole (5.3 g, 29.8 mmol) (prepared according to the method given in European Patent Publication EP 538156), salicylaldoxime (0.58 g, 4.25 mmol), 5-bromo-2-chlorotoluene (2.8 g, 21.3 mmol), copper oxide (0.15 g, 1.06 mmol) and cesium carbonate (11.8 g, 36.2 mmol) in 20 mL of N,N-dimethylformamide was heated at 140° C. overnight and then allowed to cool to room temperature. The resulting suspension was filtered and the filtrate was concentrated under reduce pressure. The resulting residue was purified by medium pressure liquid chromatography (2 to 10% gradient of ethyl acetate in hexanes as eluant) to give the title compound as a white solid (1.4 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822521B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-eb7316c064804edc9d13bdbb0e2da187
Quellennotizuspto-grants-2014_09