Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491851생성일: 2026년 10월 27일
Ethyl 2-formyl-3-oxopropanoate → 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/491851
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl 2-formyl-3-oxopropanoate | HCID 11029955 | — |
| 반응물 | 3-Hydrazino-4-methylbenzoic acid hydrochloride | HCID 56777508 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 57559708 | 68% |
반응 단계
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]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07531560B2 |
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| 출처 데이터셋 | uspto-grants-2009_05 |
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| ORD ID | ord-c22620a1782542e7943f04f163d8a864 |
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| 출처 메모 | uspto-grants-2009_05 |
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