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HRID 409734作成日:2026年10月26日

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

https://huagongshe.com/reaction/409734

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Ethoxyphenyl)pyridineHCID 70700933—
触媒Adams' catalystHCID 345198—
溶媒Acetic AcidHCID 176—
生成物4-(4-Ethoxyphenyl)piperidineHCID 21495191—
生成物THF MeOH NH4OHHCID 86686122—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759528B2
出典データセットuspto-grants-2014_06
ORD IDord-db7752a720184053b3748059490b60bf
出典メモuspto-grants-2014_06