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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1383483생성일: 2026년 10월 26일

Hydrogen Peroxide → 3,5-dichloro-4-(2-(3-cyclopentyloxy-4-methoxyphenyl)-2-oxoethyl)pyridine-N-oxide

https://huagongshe.com/reaction/1383483

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물3-Cyclopentyloxy-4-methoxyphenyl 3,5-dichloropyrid-4-ylmethyl ketoneHCID 21469578—
용매Acetic AcidHCID 176—
용매Ethyl AcetateHCID 8857—
생성물3,5-dichloro-4-(2-(3-cyclopentyloxy-4-methoxyphenyl)-2-oxoethyl)pyridine-N-oxideHCID 21187845—

반응 조건

온도80 °C

반응 단계

Aqueous 27.5% hydrogen peroxide (0.32 mL) is added to a solution of 3-cyclopentyloxy-4-methoxyphenyl 3,5-dichloropyrid-4-ylmethyl ketone (990 mg) in glacial acetic acid (13 mL). The reaction is heated at 80° C. for 8 hours then allowed to stand overnight at room temperature. A further aliquot of aqueous 27.5% hydrogen peroxide (0.32 mL) is added and the mixture heated at 80° C. for 2 hours. The reaction mixture is diluted with ethyl acetate (200 mL) and washed with saturated aqueous sodium bicarbonate until the washings remained basic. The mixture is washed with brine (50 mL), dried (MgSO4), concentrated and the residue recrystallized from a mixture of dichloromethane/ethyl acetate/heptane to give 3,5-dichloro-4-(2-(3-cyclopentyloxy4-methoxyphenyl)-2-oxoethyl)pyridine-N-oxide as a yellow solid, m.p. 179-180° C. [Elemental analysis: C,57.3; H,4.81; N,3.54; Cl,18.0%; calculated for C19H19Cl2NO4: C,57.59; H,4.83; N,3.53; Cl,1,17.89%.]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06255326B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-08ae1548604e4fa8a07314ce2bfcd269
출처 메모uspto-grants-2001_07