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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 951생성일: 2026년 10월 23일

Methanol → 4-(4-Phenoxyphenyl)piperidine

https://huagongshe.com/ko/reaction/951

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 (3) synthesized in Reference Example 3 were added 200 mg of palladium carbon and 1 ml of acetic acid for hydrogenation at atmospheric pressure and room temperature. After the end of the reaction, the insolubles were filtered off and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in methylene chloride, then adjusted by a 10% aqueous solution of sodium hydroxide to pH=9 to 10, then was shaken. The organic layer was dried, filtered, then concentrated 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-reference compound (4) in all amount of 2.32 g (yield of 66%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723475
출처 데이터셋uspto-grants-1998_03
ORD IDord-33d9f641c6034e9a99040843b1b7b174
출처 메모uspto-grants-1998_03