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HRID 491851作成日:2026年10月27日

Ethyl 2-formyl-3-oxopropanoate → 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/491851

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-formyl-3-oxopropanoateHCID 11029955—
反応物3-Hydrazino-4-methylbenzoic acid hydrochlorideHCID 56777508—
溶媒EthanolHCID 702—
生成物1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 5755970868%

反応手順

A solution of 2-formyl-3-oxo-propionic acid ethyl ester (S. H. Bertz et al., J. Org. Chem., 1982, 47, 2216) (1.44 g, 10 mmol) in EtOH (10 mL) was cooled in an ice bath. A slurry of 3-hydrazino-4-methyl-benzoic acid hydrochloride (2.02 g, 10 mmol) in EtOH (50 mL) was added and the reaction was stirred overnight. The EtOH was removed under reduced pressure and the residue partitioned between water and CH2Cl2. The layers were separated and the organic layer washed with brine. The organic layer was dried over Na2SO4, filtered, and concentrated. Hexanes were added and the solution concentrated. The resulting solid was collected by vacuum filtration, washed with hexanes and dried under vacuum to provide 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester (1.86 g, 68%) as a yellow solid: ESI MS m/z 275 [C14H14N2O4+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531560B2
出典データセットuspto-grants-2009_05
ORD IDord-c22620a1782542e7943f04f163d8a864
出典メモuspto-grants-2009_05