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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1636021생성일: 2026년 10월 25일

Pyridine → N-[2,2,2-Trifluoro-1-(4-methoxyphenyl)ethylidene]hydroxylamine

https://huagongshe.com/reaction/1636021

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Hydroxylamine HClHCID 21645—
반응물2,2,2-Trifluoro-4'-methoxyacetophenoneHCID 136555—
용매EthanolHCID 702—
생성물N-[2,2,2-Trifluoro-1-(4-methoxyphenyl)ethylidene]hydroxylamineHCID 5911515149.4%

반응 단계

10 g (49.0 mmol) of 2,2,2-trifluoro-1-(4-methoxyphenyl)-ethanone are dissolved in 100 ml of ethanol. To the solution are added 4.1 g (58.8 mmol) of hydroxylammonium chloride and 11.9 ml (147 mmol) of pyridine. The reaction mixture is refluxed for 4 hours, and the solvent is distilled off by a rotary evaporator. The residue is poured into 50 ml of water, and extracted with 100 ml and 50 ml of ethyl acetate. The organic phase is washed with potassium hydrogen sulfate aqueous solution, water, and brine, dried over MgSO4, and concentrated. The residue is purified by chromatography with methylene chloride, yielding 5.3 g of 2,2,2-trifluoro-1-(4-methoxyphenyl)-ethanone oxime as a white solid with a melting point of 62-80° C. The structure is confirmed by the 1H-NMR spectrum (CDCl3). δ [ppm]: 3.84 (s, 3H), 6.93(E)/6.99(Z) (d, 2H), 7.45(E)/7.55(Z) (d, 2H), 8.78 (br s, 1H). The signals are tentatively assigned to the E- and Z-conformations. The spectrum indicates the compound is a mixture of E- and Z-isomers. The ratio of the mixture is estimated to be E:Z=1:1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06512020B1
출처 데이터셋uspto-grants-2003_01
ORD IDord-8710df51544645639ed95bc8feef62ba
출처 메모uspto-grants-2003_01