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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265986생성일: 2026년 10월 25일

m-Chloroperbenzoic acid → [1-[2-[3-(3,4-Dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]-4-phenylpiperidine-4-carbonyl]-oxidoazanium

https://huagongshe.com/reaction/265986

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참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물4-Phenyl-1-[2-[3-(3,4-dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]piperidine-4-carboxamideHCID 9874168—
용매DichloromethaneHCID 6344—
생성물[1-[2-[3-(3,4-Dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]-4-phenylpiperidine-4-carbonyl]-oxidoazaniumHCID 88374405—

반응 조건

온도0 °C

반응 단계

Combine 1-[2-[3-(3,4-dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid amide (1.0 mmol) and dichloromethane (10 mL). Cool to 0° C. Add portionwise, m-chloroperbenzoic acid (1.0 mmol). After the addition is complete, warm to ambient temperature. After 18 hours, extract the reaction mixture with water. Separate the organic layer, dry over MgSO4, filter, and evaporate in vacuo to give a residue. Purify the residue by chromatography to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648366
출처 데이터셋uspto-grants-1997_07
ORD IDord-f0889a4a895b4b1d9f45983278db4223
출처 메모uspto-grants-1997_07