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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 462649생성일: 2026년 10월 23일

3-Hydroxypyridine → 3-Pyridyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate

https://huagongshe.com/ko/reaction/462649

반응식

참여 물질

역할이름HCID투입량
반응물3-HydroxypyridineHCID 7971—
반응물TriethylamineHCID 8471—
반응물5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—
용매TolueneHCID 1140—
생성물3-Pyridyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoateHCID 1347565670.7%

반응 단계

To a stirred solution of 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride (3.79 g, 0.01 mole) and triethyl amine (1.01 g, 0.01 mole) in toluene (50 ml) was added 3-hydroxypyridine (0.95 g, 0.01 mole). The temperature exothermed to 33° C. and there was an immediate precipitate. The reaction was then refluxed for 24 hours, cooled to room temperature and the triethylamine hydrochloride precipitate collected by filtration. The toluene solution was washed with dilute sodium hydroxide solution and then with saturated sodium chloride solution. After drying and evaporation of the solvent there was obtained 3.1 g of brown oil which solidified. This was triturated with hexane and the solid filtered and dried to give a tan product, m.p. 65°-68° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04517010
출처 데이터셋uspto-grants-1985_05
ORD IDord-db7961b217924eacadb71753c875ceb0
출처 메모uspto-grants-1985_05