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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303944Generated: October 30, 2026

4-Cyano-4-(3,4-dichlorophenyl)-7-(tetrahydropyran-4-yloxy)-heptanoic Acid Ethyl Ester → 5-(3,4-Dichlorophenyl)-5-[3-(tetrahydropyran-4-yloxy)-propyl]-2-piperidone

https://huagongshe.com/reaction/2303944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyano-4-(3,4-dichlorophenyl)-7-(tetrahydropyran-4-yloxy)-heptanoic Acid Ethyl EsterHCID 15887652—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventAmmonium HydroxideHCID 14923—
Product5-(3,4-Dichlorophenyl)-5-[3-(tetrahydropyran-4-yloxy)-propyl]-2-piperidoneHCID 1588765384.8%

Reaction Steps

Raney Ni is added to a solution of cyanoester (5) (8.5 g, 19.84 mmol) in absolute EtOH (200 mL) and concentrated NH4OH (40 mL), The mixture was subjected to a H2 (51.8 psi) Par for 64.5 hours. The reaction mixture was filtered through celite, and N2 gas was passed through the solution to remove NH3. EtOH was then evaporated, and water is azeotropically removed with toluene. The crude oil is purified by flash chromatography (Ch2Cl2—MeOH/95:5) to give a colorless solid (6.5 g, 84.8% yield), mp ˜45° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433178B1
Source datasetuspto-grants-2002_08
ORD IDord-2656c94dfb4c44eaa8a75dced90ad577
Source noteuspto-grants-2002_08