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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285916Generated: October 25, 2026

Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl- → Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-

https://huagongshe.com/reaction/2285916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl-HCID 3060390—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductPiperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-HCID 306039250.3%

Reaction Steps

A solution of 1-methyl-4-(4-nitrophenoxy)-4-phenylpiperidine (4.4 g, 14.1 mM) in methanol (250 ml) was hydrogenated at 1 atmosphere and ambient temperature over 5% palladium on charcoal (500 mg) until the theoretical uptake of hydrogen had occurred (about 2 hours). The catalyst was removed by filtration and the solvent evaporated under reduced pressure. Recrystallisation of the residue from IPA gave the title compound (2 g) m.p. 174°-5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04325953
Source datasetuspto-grants-1982_04
ORD IDord-087ae6c0a6d144b4b3419ed8322470da
Source noteuspto-grants-1982_04