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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41958생성일: 2026년 10월 26일

Pyridine → 3'-Fluoro-4'-methoxyacetophenone-o-3-fluorobenzyloxime

https://huagongshe.com/reaction/41958

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물1-(3-Fluoro-4-methoxyphenyl)ethan-1-oneHCID 96828—
반응물o-(3-Fluorobenzyl)hydroxylamine hydrochlorideHCID 23206139—
용매EthanolHCID 702—
생성물3'-Fluoro-4'-methoxyacetophenone-o-3-fluorobenzyloximeHCID 8713866590.1%

반응 단계

A solution of 3-fluoro-4-methoxyacetophenone (0.063 g, 0.377 mmol), O-(3-fluorobenzyl)hydroxylamine hydrochloride (0.100 g, 0.569 mmol) and pyridine (0.14 ml, 1.73 mmol) in ethanol (5 ml) was stirred at reflux under nitrogen for 4 h and cooled to room temperature. The solution was concentrated to a pale yellow oil which was diluted with water. The suspension was extracted with dichloromethane (×3). The combined organic phases were washed with water and brine, dried over magnesium sulphate, filtered and concentrated to a white solid. The crude product was purified by column chromatography (SiO2), eluting with 95:5 petrol/ethyl acetate, to give 3′-fluoro-4′-methoxyacetophenone-O-3-fluorobenzyloxime (CP9-126) as a white solid (0.099 g, 90%), m.p. 67°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536157B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5b90820628314994913bf3c02418e6c9
출처 메모uspto-grants-2013_09