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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 839228Erstellt: 23. Oktober 2026

Phosphorus oxychloride → 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/de/reaction/839228

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
Edukt3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonyl chlorideHCID 20325933—
Edukt3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 20325964—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamideHCID 20326123—

Reaktionsschritte

Heat 1 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid together with 0.56 g of phosphorus oxychloride and 10 ml of dichloroethane for 2 hours at 80° C. Add 10 ml of a 25% aqueous solution dropwise at 0° C to the thus-obtained solution of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic chloride. Allow the resulting mixture to stand overnight and then vacuum distil it to remove the organic solvent therefrom. Vacuum filter to separate formed precipitate and recrystallize the filter residue from dimethylformamide/methanol to obtain 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxamide [m.p. 236° to 238° C].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04093812
Quelldatensatzuspto-grants-1978_06
ORD IDord-5d8967682a2c4ddfacb5de96cc45fbc9
Quellennotizuspto-grants-1978_06