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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1617314생성일: 2026년 10월 27일

4-(4-Ethoxyphenyl)pyridine → 4-(4-Ethoxyphenyl)piperidine

https://huagongshe.com/reaction/1617314

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Ethoxyphenyl)pyridineHCID 70700933—
촉매Adams' catalystHCID 345198—
용매Acetic AcidHCID 176—
생성물4-(4-Ethoxyphenyl)piperidineHCID 21495191—
생성물THF MeOH NH4OHHCID 86686122—

반응 단계

410 mg (2.06 mmol) 4-(4-Ethoxy-phenyl)-pyridine in 10 mL acetic acid are hydrogenated (3 bar) for 9 h at rt using 50 mg platinum(IV) oxide. After that time, the catalyst is filtered off and the solvent is evaporated. The residue is taken up in 1N NaOH and extracted with EtOAc. The organic layer is dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silica gel; DCM:MeOH 9:1, then THF:MeOH:NH4OH 1:1:0.1) to yield the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765959B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-3e63012b4679453eb9937d612c2d2af2
출처 메모uspto-grants-2014_07