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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399174Generated: October 31, 2026

4-(N-Propionylaniline)piperidine → HCID 131710806, compound

https://huagongshe.com/reaction/2399174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Propionylaniline)piperidineHCID 259381—
ReactantHCID 131710807HCID 131710807—
SolventCyclohexaneHCID 8078—
ProductHCID 131710806HCID 131710806—

Reaction Steps

Using the procedure of Example I step B and starting from (α-naphtoxyethyl) bromide and 4(N-phenyl N-propionylamino) piperidine, N(α-naphtoxyethyl) 4-(N'-phenyl-N'-propionylamino) piperidine is obtained melting at 110°-112° (cyclohexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04027028
Source datasetuspto-grants-1977_05
ORD IDord-89b4f108da6a46ab9c380e5711fa6c74
Source noteuspto-grants-1977_05