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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66681생성일: 2026년 10월 26일

Hydrochloric Acid → 1-Acetyl-4-(2-fluoro-4-methoxybenzoyl)-piperidine

https://huagongshe.com/reaction/66681

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물3-FluoroanisoleHCID 9975—
반응물1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichloroethaneHCID 11—
생성물1-Acetyl-4-(2-fluoro-4-methoxybenzoyl)-piperidineHCID 20530719—

반응 단계

A mixture of 155 parts of 1-fluoro-3-methoxybenzene, 75 parts of aluminium chloride and 650 parts of 1,2-dichloroethane is stirred and 113 parts of 1-acetyl-4-piperidinecarbonyl chloride are added portionwise. Upon completion, stirring is continued for 1 hour at 40°-50° C. The reaction mixture is poured onto a mixture of crushed ice and hydrochloric acid. The product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is purified by high pressure liquid-chromatography over silica gel using a mixture of trichloromethane, hexane and methanol (47.5:47.5:5 by volume) as eluent. The first fraction (A-isomer) is collected and the eluent is evaporated, yielding 1-acetyl-4-(2-fluoro-4-methoxybenzoyl)-piperidine. The second fraction (B-isomer) is collected and the eluent is evaporated, yielding 40 parts (25%) of 1-acetyl-4-(4-fluoro-2-hydroxybenzoyl)piperidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04342870
출처 데이터셋uspto-grants-1982_08
ORD IDord-244f7262034a42db9b85dfa651d4a2a8
출처 메모uspto-grants-1982_08