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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526701생성일: 2026년 10월 25일

Sulfuric Acid → 1-(2,4-dichloro-phenyl)-4-methyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/526701

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물(2,4-Dichlorophenyl)hydrazine monohydrochlorideHCID 2723905—
반응물Lithium 3-ethoxycarbonyl-2-methyl-3-oxo-1-(4-trifluoromethyl-phenyl)-propan-1-olateHCID 89907367—
용매EthanolHCID 702—
생성물1-(2,4-dichloro-phenyl)-4-methyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazole-3-carboxylic acidHCID 44191746—

반응 단계

A solution of 10 g of Lithium 3-ethoxycarbonyl-2-methyl-3-oxo-1-(4-trifluoromethyl-phenyl)-propan-1-olate, 6.9 g of (2,4-Dichloro-phenyl)-hydrazine hydrochloride and 74 ml of sulfuric acid (50%) in 184 ml of ethanol was heated to reflux for 7 h. After cooling to room temperature the organic solvents were removed under reduced pressure and the residue was diluted with 100 ml of water and extracted with ethyl acetate. The combined organic layers were dried over MgSO4 and the solvent was removed under reduced pressure. The residue was dissolved in 100 ml THF and a solution of 1.4 g of LiOH in 20 ml water was added at room temperature. The reaction mixture was heated to 60° C. for 7 h. Then, after cooling to room temperature the mixture was acidified to pH 1 by addition of half-concentrated hydrochloric acid. The precipitating product was collected by filtration and washed with water. The residue was codistilled twice with dichloromethane and twice with toluene. The isolated crude product was used in the next reaction step. Yield: 13 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346762B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-97cda890ab2e45d5b4e65d5cd486ebe9
출처 메모uspto-grants-2016_05