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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52219생성일: 2026년 10월 24일

Dimethylformamide → 3-(2-chloro-6-fluorophenyl)-5-[3-chloro-4-(2-chloro-4-trifluoromethylphenoxymethyl)phenyl]-1-methyl-1H-1,2,4-triazole

https://huagongshe.com/ko/reaction/52219

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-4-(trifluoromethyl)phenolHCID 2736603—
반응물5-(4-bromomethyl-3-chlorophenyl) 3-(2-chloro-6-fluorophenyl)-1-methyl-1H-1,2,4-triazoleHCID 21463648—
용매WaterHCID 962—
생성물3-(2-chloro-6-fluorophenyl)-5-[3-chloro-4-(2-chloro-4-trifluoromethylphenoxymethyl)phenyl]-1-methyl-1H-1,2,4-triazoleHCID 2146364679.5%

반응 단계

To 30 ml of N,N-dimethylformamide are added 2-chloro-4-trifluoromethyl phenol (0.29 g) and potassium carbonate (0.25 g) and 5-(4-bromomethyl-3-chlorophenyl) 3-(2-chloro-6-fluorophenyl)-1-methyl-1H-1,2,4-triazole (0.60 g) is added thereto at room temperature with stirring, which is stirred at 120° C. for 1 hour. On completion of the reaction, the reaction solution is cooled to room temperature, poured into water and extracted with toluene. 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 0.61 g of desired compound (melting point: 113.0°-114.0° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616594
출처 데이터셋uspto-grants-1997_04
ORD IDord-54b24907367e43bb8e1680fedf842868
출처 메모uspto-grants-1997_04