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HRID 839229作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxamideHCID 20326123—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 20325964—

反応手順

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].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04093812
出典データセットuspto-grants-1978_06
ORD IDord-71bf263e3d2d4cb9bb67cdc13d1fef06
出典メモuspto-grants-1978_06