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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52242생성일: 2026년 10월 24일

3-Chloro-p-toluonitrile → 3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazole

https://huagongshe.com/ko/reaction/52242

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참여 물질

역할이름HCID투입량
반응물3-Chloro-p-toluonitrileHCID 88894—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chlorideHCID 54347086—
용매1,2-DichlorobenzeneHCID 7239—
생성물3-(2-chloro-6-fluorophenyl)-5-(3-chloro-4-methylphenyl) 1-methyl-1H-1,2,4-triazoleHCID 2146364755.1%

반응 조건

온도140 °C

반응 단계

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (7.50 g), 3-chloro-4-methylbenzonitrile (3.33 g), anhydrous aluminum chloride (3.00 g) and o-dichlorobenzene (20 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, it is washed with saline. Then, it is 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 3.70 g of desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616594
출처 데이터셋uspto-grants-1997_04
ORD IDord-d09da8cf964749938e77b8540c98d8c7
출처 메모uspto-grants-1997_04