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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl 2-formyl-3-oxopropanoate | HCID 11029955 | — |
| 反応物 | 3-Hydrazino-4-methylbenzoic acid hydrochloride | HCID 56777508 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 57559708 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07531560B2 |
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| 出典データセット | uspto-grants-2009_05 |
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| ORD ID | ord-c22620a1782542e7943f04f163d8a864 |
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| 出典メモ | uspto-grants-2009_05 |
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