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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448298Generated: November 2, 2026

1-Benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amine → 4-(Methoxymethyl)-N-phenylpiperidin-4-amine

https://huagongshe.com/reaction/1448298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amineHCID 3047724—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product4-(Methoxymethyl)-N-phenylpiperidin-4-amineHCID 18319932—

Reaction Steps

A mixture of 10 parts of 4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine and 200 parts of acetic acid is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The oily residue is dissolved in water, cooled and alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silicagel using a mixture of trichloromethane and 10% of methanol, saturated with gaseous ammonia, as eluent. The pure fractions are collected and the eluent is evaporated, yielding 4-(methoxymethyl)-N-phenyl-4-piperidinamine as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-f4fb923376b14062836fafd8b6f95b96
Source noteuspto-grants-1979_12