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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 654134생성일: 2026년 10월 26일

Sodium ethoxide → Chlorfenapyr

https://huagongshe.com/reaction/654134

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ethoxideHCID 2723922—
반응물4-Bromo-1-(chloromethyl)-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrileHCID 19888616—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물ChlorfenapyrHCID 9177885.9%

반응 단계

A solution of 4-bromo-1-(chloromethyl)-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carbonitrile (2.0 g, 0.005 mol) in absolute ethanol is treated with a 21% wt/wt ethanolic solution of sodium ethoxide (0.36 g, 0.0053 mol), heated to 75°-80° C. for 20-30 minutes, cooled to room temperature and diluted with water and ether. The organic phase is dried over anhydrous magnesium sulfate and concentrated in vacuo to give a solid which is recrystallized form heptane to give the title product as a white solid (1.75 g, mp 97°-98° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05130328
출처 데이터셋uspto-grants-1992_07
ORD IDord-d87701a3380848998d4943e36ed4b71b
출처 메모uspto-grants-1992_07