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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12867생성일: 2026년 10월 23일

Dichloromethane → Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/ko/reaction/12867

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물tert-Butylhydrazine monohydrochlorideHCID 81889—
반응물Sodium AcetateHCID 517045—
반응물Methyl 2-((dimethylamino)methylene)-3-oxobutanoateHCID 53395488—
용매EthanolHCID 702—
생성물Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylateHCID 5085323071%

반응 조건

온도90 °C

반응 단계

A solution of 2-dimethylaminomethylene-3-oxo-butyric acid methyl ester (7.43 g, 43.40 mmol) in absolute ethanol (70 mL) was treated with tert-butylhydrazine hydrochloride (5.52 g, 44.29 mmol) and sodium acetate (4.42 g, 53.88 mmol). The resulting mixture was heated to 90° C. for 18 h. At this time, the reaction was cooled to 25° C. The reaction was poured onto ice using dichloromethane to assist the transfer (50 mL). The mixture was transferred to a separatory funnel at which time the layers were shaken and separated. The aqueous layer was further extracted with dichloromethane (1×50 mL). The combined organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL), water (1×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. ISCO CombiFlash (120 g column; 0-10% ethyl acetate/hexanes) afforded 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid methyl ester (6.04 g, 71%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728029B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5c72efe1e923436eb6ffc65c2c606b2c
출처 메모uspto-grants-2010_06