Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704440Generated: October 30, 2026

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

https://huagongshe.com/reaction/1704440

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 numberUS04126689
Source datasetuspto-grants-1978_11
ORD IDord-52d9a27123584a58a4ee9fbb9086681c
Source noteuspto-grants-1978_11