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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236777Generated: October 26, 2026

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

https://huagongshe.com/reaction/236777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantN,N-DiethylacetamideHCID 12703—
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-diethylethanamide 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 numberUS04157393
Source datasetuspto-grants-1979_06
ORD IDord-3cb8a07bc3fd4993b51c0996b0c2daab
Source noteuspto-grants-1979_06