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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52225생성일: 2026년 10월 23일

Water → 3-(2-chloro-6-fluorophenyl)-5-[2-chloro-4-(3-chloro-5-trifluoromethylpyridine-2-yloxymethyl)phenyl]-1-methyl-1H-1,2,4-triazole

https://huagongshe.com/ko/reaction/52225

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
반응물3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-hydroxymethylphenyl) 1-methyl-1H-1,2,4-triazoleHCID 21463618—
용매1,2-DimethoxyethaneHCID 8071—
생성물3-(2-chloro-6-fluorophenyl)-5-[2-chloro-4-(3-chloro-5-trifluoromethylpyridine-2-yloxymethyl)phenyl]-1-methyl-1H-1,2,4-triazoleHCID 2146368082.1%

반응 조건

온도0 °C

반응 단계

3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-hydroxymethylphenyl) 1-methyl-1H-1,2,4-triazole (0.50 g) is dissolved in 1,2-dimethoxyethane (20 ml) and cooled to 0° C., to which is added sodium hydride (60%, 0.07 g) and the reaction mixture is stirred for 15 minutes. Then, a solution of 2,3-dichloro-5-trifluoromethyl pyridine (0.34 g) in 1,2-dimethoxyethane (10 ml) is added dropwise and stirred for 3 hours. On completion of the reaction, the reaction solution is warmed to room temperature and poured into water and extracted with ether. The organic layer is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography to give 0.62 g of desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616594
출처 데이터셋uspto-grants-1997_04
ORD IDord-a27c64c90b344b65971f5c1a125fed1a
출처 메모uspto-grants-1997_04