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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1011616생성일: 2026년 10월 26일

4-(Trifluoromethyl)benzenesulfonamide → N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamide

https://huagongshe.com/reaction/1011616

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzenesulfonamideHCID 70018—
반응물3-Iodo-1-(methoxymethyl)-1H-pyrazole-4-carbaldehydeHCID 57659764—
촉매Titanium tetraethoxideHCID 76524—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamideHCID 67313312—

반응 단계

3-Iodo-1-(methoxymethyl)-1H-pyrazole-4-carbaldehyde (39) (2.0 g, 7.52 mmol) and 4-(trifluoromethyl)benzenesulfonamide (40) (1.69 g, 7.52 mmol) were dissolved in THF (20 mL) under nitrogen. Titanium(IV) ethoxide (7.8 mL, 37.6 mmol) was added via syringe and the reaction stirred for 16 hr at rt. The reaction was poured into brine (50 mL) and filtered through a pad of Celite. The filtrate was extracted with EtOAc (3×50 mL) and the combined organics were washed with brine (100 mL), dried over Na2SO4, and concentrated in vacuo to give N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamide (41) as a clear oil that was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07977368B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-18b12a13eaee4612ab3c910786c31e50
출처 메모uspto-grants-2011_07