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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55744생성일: 2026년 10월 24일

Potassium Iodide → Tyclopyrazoflor

https://huagongshe.com/ko/reaction/55744

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Ethyl BromideHCID 6332—
반응물Sodium hydrideHCID 24758—
반응물N-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)-3-((3,3,3-trifluoropropyl)thio)propanamideHCID 86700584—
용매SulfolaneHCID 31347—
생성물TyclopyrazoflorHCID 86700627—

반응 단계

To 3-neck round bottomed flask (50 mL) was added sodium hydride (60% in oil, 0.130 g, 3.28 mmol) and sulfolane (16 mL). The gray suspension was stirred for 5 minutes then N-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)-3-((3,3,3-trifluoropropyl)thio)propanamide (1.20 g, 3.16 mmol) dissolved in sulfolane (25 mL) was slowly added dropwise over 5 minutes. The mixture became a light gray suspension after 3 minutes and was allowed to stir for 5 minutes after which time ethyl bromide (0.800 mL, 10.7 mmol) and potassium iodide (0.120 g, 0.720 mmol) were added sequentially. The cloudy suspension was then allowed to stir at room temperature. The reaction was quenched after 6 hours by being poured drop-wise into cooled ammonium formate/acetonitrile solution (30 mL). The resulting orange colored solution was stirred and tetrahydrofuran (40 mL) was added. The mixture was assayed, using octanophenone as a standard, and found to contain (1.09 g, 85%) of the desired product with a selectivity versus the retro-Michael-like decomposition product of 97:3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09433215B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8c178e7cd78948a2aefcc4ac48964a1b
출처 메모uspto-grants-2016_09