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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549403Generated: October 29, 2026

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

https://huagongshe.com/reaction/549403

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 numberUS07943652B2
Source datasetuspto-grants-2011_05
ORD IDord-bc8f167e016942a4a35010e6b8e2f49a
Source noteuspto-grants-2011_05