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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1617314Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1617314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(4-Ethoxyphenyl)pyridineHCID 70700933—
KatalysatorAdams' catalystHCID 345198—
LösungsmittelAcetic AcidHCID 176—
Produkt4-(4-Ethoxyphenyl)piperidineHCID 21495191—
ProduktTHF MeOH NH4OHHCID 86686122—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08765959B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-3e63012b4679453eb9937d612c2d2af2
Quellennotizuspto-grants-2014_07