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HRID 569709Erstellt: 24. Oktober 2026

Pyridine → 5-(2,4-Dichlorophenoxyacetamido)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole

https://huagongshe.com/de/reaction/569709

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt(2,4-Dichlorophenoxy)acetyl chlorideHCID 69887—
Edukt5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazoleHCID 13557109—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(2,4-Dichlorophenoxyacetamido)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazoleHCID 1391173994,3%

Reaktionsschritte

2.2 ml (0.0275 mol) of anhydrous pyridine and 6.7 g (0.027 mol) of 96.3 percent strength 2,4-dichlorophenoxyacetyl chloride are added successively to 8 g (0.027 mol) of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole (cf. U.S. Pat. No. 4,614,533, supra, in 60 ml of dichloromethane with stirring at 0° C. to 5° C. and the mixture is stirred for 16 hours at room temperature. The mixture is worked up by adding 100 ml of dichloromethane, washing successively with dilute hydrochloric acid, saturated sodium bicarbonate solution and saturated sodium chloride solution, drying the organic phase over magnesium sulphate and removing the solvent in vacuo. 12.7 g (94.3% of theory) of 5-(2,4-dichlorophenoxyacetamido)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole of melting point 167° C.-180° C. are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04734125
Quelldatensatzuspto-grants-1988_03
ORD IDord-55b6c277f7e24b56919f2ba491507085
Quellennotizuspto-grants-1988_03