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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802776Generated: November 1, 2026

Methyl iodide → 3-(4-Bromo-phenyl)-1-methyl-piperazine

https://huagongshe.com/reaction/1802776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(4-Bromophenyl)piperazineHCID 21838686—
SolventAcetoneHCID 180—
Product3-(4-Bromo-phenyl)-1-methyl-piperazineHCID 5789922746.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 2-(4-bromophenyl)piperazine (4.07 g, 16.0 mmol) and triethylamine (17 mL, 122 mmol) in acetone (50 mL) was added a solution of methyl iodide (1.4 mL, 22 mmol) in acetone (20 mL) over 50 min and the reaction mixture was stirred at 0° C. for 15 minutes, warmed to room temperature, and stirred for 16 h. The reaction mixture was slowly treated with saturated ammonium chloride (150 mL) and extracted with ethyl acetate (200 mL×3). The organic layers were combined, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification via flash silica gel column chromatography (heptane/ethyl acetate) gave 3-(4-bromo-phenyl)-1-methyl-piperazine (1.89 g, 46% yield). LCMS (m/z): 257.00 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349883B2
Source datasetuspto-grants-2013_01
ORD IDord-7be4b9ce46754c03853998d73cba79e3
Source noteuspto-grants-2013_01