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HRID 1617314作成日:2026年10月25日

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

https://huagongshe.com/reaction/1617314

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US08765959B2
出典データセットuspto-grants-2014_07
ORD IDord-3e63012b4679453eb9937d612c2d2af2
出典メモuspto-grants-2014_07