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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432205Generated: October 25, 2026

N-Methyl-N-phenylbenzylamine → N-benzyl-N-(4-bromophenyl)-N-methylamine

https://huagongshe.com/reaction/432205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-N-phenylbenzylamineHCID 69191—
Reactant2,4,4,6-Tetrabromocyclohexa-2,5-dienoneHCID 88433—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-N-(4-bromophenyl)-N-methylamineHCID 2234739256.7%

Reaction Steps

N-benzyl-N-phenyl-N-methylamine (4.41 g, 0.0224 mol) was dissolved in anhydrous dichloromethane (150 mL) and 2,4,4,6-tetrabromocyclohexadiene-1-one(9.16 g, 0.0224 mol) was added in 10 equal portions over a 30 min. period. Stirring was continued at ambient temperature for 20 hours. The organic phase was successively washed with 0.5N solution of sodium hydroxide in water (100 mL), 1N solution of sodium hydroxide in water (100 mL), water (120 mL) and brine (120 mL). The organic phase was dried with magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (1:99) as mobile phase to yield N-benzyl-N-(4-bromophenyl)-N-methylamine (3.52 g, 0.0127 mol) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-b4d0e4dee0fc4432b379558712d568b2
Source noteuspto-grants-2003_12