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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1274345생성일: 2026년 10월 26일

Water → 3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(4,4-diethoxy-1-hydroxybut-2-ynyl)pyrazole

https://huagongshe.com/reaction/1274345

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Propane, 1,1-diethoxy-HCID 20858—
반응물3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)4-formylpyrazoleHCID 18417981—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(4,4-diethoxy-1-hydroxybut-2-ynyl)pyrazoleHCID 22120899—

반응 단계

To a solution of propionaldehyde diethyl acetal (0.0192 g) in anhydrous tetrahydrofuran (2 ml) cooled to -78° C. under an atmosphere of nitrogen was added dropwise n-butyl lithium (62 μl, 2.5M in hexanes) and the mixture was stirred for 10 minutes. 3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-formylpyrazole (0.05 g) was added and stirring continued for 30 minutes. The reaction mixture was poured into water (5 ml) and ether (5 ml). The organic layer was separated, dried (Na2SO4) and evaporated. The residue was purified by column chromatography on silica gel (5 g) eluted with dichloromethane. Combination and evaporation of suitable fractions gave the title compound as a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06156782
출처 데이터셋uspto-grants-2000_12
ORD IDord-ae28a78715e74c5ba7e345251b549238
출처 메모uspto-grants-2000_12