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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049616Generated: November 3, 2026

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

https://huagongshe.com/reaction/2049616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
Reactant1-Benzyl-4-(phenylamino)piperidine-4-methanolHCID 3017230—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
Product1-Benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amineHCID 3047724—

Reaction Steps

To a solution of 32 parts of 4-(phenylamino)-1-(phenylmethyl)-4-piperidinemethanol in 90 parts of benzene are added 0.2 parts of N,N,N-triethylbenzenemethanaminium chloride and 150 parts of a sodium hydroxide solution 60%. After stirring vigourously, there are added dropwise 10.9 parts of dimethylsulfate at a temperature below 30° C. Upon completion, stirring is continued at room temperature, first for 2h.30 and further, after the addition of a second portion of 2.6 parts of dimethyl sulfate, for 1h.30. The reaction mixture is cooled in ice-water and 200 parts of water are added. The organic phase is separated and the aqueous phase is extracted with benzene. The combined organic phases are washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 3% of methanol, saturated with ammonia, as eluent. The pure fractions are collected and the eluent is evaporated, yielding 24.8 parts of 4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198411
Source datasetuspto-grants-1980_04
ORD IDord-812f5c85fbae4d909fde1a64f69d91ba
Source noteuspto-grants-1980_04