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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891148Generated: November 2, 2026

Methyl iodide → 1-(4-Bromophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/1891148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Bromophenyl)piperazineHCID 2735629—
SolventDimethylformamideHCID 6228—
Product1-(4-Bromophenyl)-4-methylpiperazineHCID 1181767573%

Reaction Steps

1-(4-Bromo-phenyl)-piperazine (1 g, 4.1 mmol) and potassium carbonate (1.8 g, 3 eq) in DMF (15 ml) treated with methyl iodide (250 μl, 1.1 equivalents), solution stirred at room temperature overnight. Reaction quenched with deionised water (10 ml), extracted with ethyl acetate. Organic phase washed with sodium hydrogen carbonate to remove any dimethylated impurity, dried and solvent removed to give 1-(4-Bromo-phenyl)-4-methyl-piperazine in 73% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507480B2
Source datasetuspto-grants-2013_08
ORD IDord-4d4b75024b6341e8ac0e2dc885ab75f2
Source noteuspto-grants-2013_08