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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1980405생성일: 2026년 10월 26일

4-(5-Trifluoromethyl-pyridin-2-yloxy)-phenol → 2-Hydroxyphenoxy-5-trifluoromethyl pyridine

https://huagongshe.com/reaction/1980405

반응식

참여 물질

역할이름HCID투입량
반응물4-(5-Trifluoromethyl-pyridin-2-yloxy)-phenolHCID 155241—
반응물Pyridine, 2-(4-methoxyphenoxy)-5-(trifluoromethyl)-HCID 155242—
용매Acetic AcidHCID 176—
용매Hydrogen BromideHCID 260—
생성물2-Hydroxyphenoxy-5-trifluoromethyl pyridineHCID 20402822—

반응 단계

2-p-Methoxyphenoxy-5-trifluoromethylpyridine (10.5 g) in glacial acetic acid (100 ml) and 48% hydrobromic acid (50 ml) were stirred and heated under reflux for 71/2 hours. The solution was then evaporated and the remaining oil treated with sodium bicarbonate solution and shaken with ether (2×300 ml). The ether extract was shaken with 2-molar sodium hydroxide solution (200 ml) and then water (150 ml). The aqueous layers were combined, acidified with 2-molar hydrochloric acid and extracted with ether (2×300 ml). The ether extract was dried and evaporated to give a brown oil identified as 2-p-hydroxyphenoxy-5-trifluoromethylpyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04508907
출처 데이터셋uspto-grants-1985_04
ORD IDord-748fdbcf9734406080217112f92e468b
출처 메모uspto-grants-1985_04