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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 839229Erstellt: 25. Oktober 2026

3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamide → 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/839229

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamideHCID 20326123—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produkt3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 20325964—

Reaktionsschritte

Add 2 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxamide to 4.7 ml of concentrated sulfuric acid while cooling on ice and then add thereto a solution of 0.78 g of sodium nitrite in 2 ml of water slowly and dropwise at a temperature not exceeding 7° C. Allow the resulting mixture to stand overnight; dilute with from 4 to 5 ml of concentrated sulfuric acid and then mix it (while cooling with ice) with 0.39 g of sodium nitrite in 1 ml of water. Allow the thus-prepared solution to stand at a temperature of 0° to 5° C for 2 days in a refrigerator and then pour it onto ice. Vacuum filter to separate formed precipitate and chromatograph with chloroform/ethanol (9:1) on a silica gel column to obtain 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid [m.p. 250° to 252° C].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04093812
Quelldatensatzuspto-grants-1978_06
ORD IDord-71bf263e3d2d4cb9bb67cdc13d1fef06
Quellennotizuspto-grants-1978_06