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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387973Generated: October 30, 2026

N-Methylcyclohexylamine → N-cyclohexyl-N-methyl-N-(4-nitrobenzyl)amine

https://huagongshe.com/reaction/1387973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Nitrobenzyl bromideHCID 66011—
SolventDimethylformamideHCID 6228—
ProductN-cyclohexyl-N-methyl-N-(4-nitrobenzyl)amineHCID 75729199.9%

Reaction Steps

In DMF (50 ml) was dissolved N-cyclohexyl-N-methylamine (12.5 g, 0.11 mol), and to the solution were added potassium carbonate (27.6 g, 0.20 mol) and 4-nitrobenzylbromide (21.6 g, 0.10 mol). The mixture was stirred at room temperature for 5 hours. Under reduced pressure, the reaction mixture was concentrated. To the residue was added ethyl acetate, and the mixture was extracted with water. The ethyl acetate layer was washed with saturated sodium chloride solution, dried with MgSO4 and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (ethyl acetate/hexane) to give N-cyclohexyl-N-methyl-N-(4-nitrobenzyl)amine (24.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-9ff653418981445ea2a41e242de15eee
Source noteuspto-grants-2001_07