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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448333Generated: November 2, 2026

2-Bromopropane → 4-(Methoxymethyl)-N-phenyl-1-(propan-2-yl)piperidin-4-amine

https://huagongshe.com/reaction/1448333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantTriethylamineHCID 8471—
Reactant4-(Methoxymethyl)-N-phenylpiperidin-4-amineHCID 18319932—
SolventDimethylacetamideHCID 31374—
Product4-(Methoxymethyl)-N-phenyl-1-(propan-2-yl)piperidin-4-amineHCID 2333904042.6%

Reaction Steps

A mixture of 10 parts of 2-bromopropane, 9 parts of 4-(methoxymethyl)-N-phenyl-4-piperidinamine, 4.9 parts of N,N-diethylethanamine and 72 parts of N,N-dimethylacetamide is stirred and refluxed for 10.25 hours. After cooling, the formed N,N-diethylethanamine hydrobromide is filtered off and the filtrate is diluted with water. The product is extracted with methylbenzene. The extract is washed thoroughly with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 5.7 parts (42.6%) of 4-(methoxymethyl)-1-(1-methylethyl)-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-32d1c8687e904c7d82c4e93e40fc4e4f
Source noteuspto-grants-1979_12