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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 992363생성일: 2026년 10월 26일

Methanol → 4-(4-Phenoxyphenyl)piperidine

https://huagongshe.com/reaction/992363

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-(4-Phenoxyphenyl)-1,2,3,6-tetrahydropyridineHCID 22599989—
촉매HCID 178418390HCID 178418390—
용매Acetic AcidHCID 176—
생성물4-(4-Phenoxyphenyl)piperidineHCID 1107598466%

반응 단계

To a 100 ml methanol solution of 3.51 g of the compound (8) synthesized in Example 1 were added 200 mg of palladium carbon and 1 ml of acetic acid for hydrogenation at atmospheric pressure and room temperature. After the completion of the reaction, the insolubles were filtered off, then the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in methylene chloride and adjusted by a 10% aqueous solution of sodium hydroxide to a pH 9 to 10, then was shaken. The organic layer was dried, filtered, then condensed under reduced pressure to obtain a residue which was then purified by silica gel column chromatography (methylene chloride:methanol=20:1) to obtain the above-referenced compound (9) in an amount of 2.32 g (yield 66%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06469010B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-68b176c97cf44b6fa785f4d2168d0504
출처 메모uspto-grants-2002_10