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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52206생성일: 2026년 10월 23일

1,2-Dichlorobenzene → 3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-nitrophenyl) 1-methyl-1H-1,2,4-triazole

https://huagongshe.com/ko/reaction/52206

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참여 물질

역할이름HCID투입량
반응물1,2-DichlorobenzeneHCID 7239—
반응물2-Chloro-4-nitrobenzonitrileHCID 141401—
반응물N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chlorideHCID 54347086—
촉매Iron chloride (FeCl3)HCID 24380—
용매ChloroformHCID 6212—
생성물3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-nitrophenyl) 1-methyl-1H-1,2,4-triazoleHCID 21463604118.3%

반응 조건

온도140 °C

반응 단계

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (1.90 g), 2-chloro-4-nitrobenzonitrile (1.80 g), anhydrous iron (III) chloride (1.60 g) and o-dichlorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, the reaction mixture is dissolved in chloroform (100 ml), washed with dilute hydrochloric acid, dilute aqueous solution of sodium hydroxide and saline in this order, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography using mixed solvent of hexane-ethyl acetate as eluent to give 2.20 g of desired compound (melting point: 144.0°-148.0° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616594
출처 데이터셋uspto-grants-1997_04
ORD IDord-d9ee018728f746e7a5dd5c3746938ef1
출처 메모uspto-grants-1997_04