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HRID 1093597作成日:2026年10月26日

Acetic Acid → HCID 178468617、化合物

https://huagongshe.com/reaction/1093597

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物2,4-Dioxo-4-phenyl-butyric acid ethyl esterHCID 226503—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
生成物HCID 178468617HCID 17846861788%

反応手順

A solution of 2,4-dioxo-4-phenyl-butyric acid ethyl ester (1.68 g, 0.0076 mole), acetic acid (10 mL) and hydrazine hydrate (0.42 g, 0.0083 mole) was heated to reflux for 5 hours. The reaction mixture was then poured into iced water, basified with saturated aqueous NaHCO3 solution and the product was extracted with ethyl acetate. The ethyl acetate layer was collected and washed with brine solution, dried over sodium and concentrated under reduced pressure. The resulting residue was purified by column chromatography using basic aluminium oxide (50% ethyl acetate in hexane) to afford 1.442 g (88%) of 5-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester. LCMS: 217.09 (M+1)+, 97.92%. To a stirred solution of 5-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester (1.4 g, 0.00667 mol) in a mixture of THF (30 mL), methanol (15 mL) and H2O (10 mL) was added LiOH.H2O (0.839 g, 0.0199 mol) at ambient temperature. The resulting mixture was stirred at 45° C. overnight. Volatiles were evaporated and the residue was diluted with water, acidified with concentrated HCl solution and the product was extracted with ethyl acetate. The ethyl acetate layer was collected, dried over sodium sulfate and concentrated under reduced pressure to afford 1.26 g (86%) of 5-phenyl-1H-pyrazole-3-carboxylic acid. LCMS: 189.06 (M+1)+, 97.7%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129376B2
出典データセットuspto-grants-2012_03
ORD IDord-13b8d5ceb1d947f8bec300bdc587e6de
出典メモuspto-grants-2012_03