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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267973Generated: October 26, 2026

2-Methylpiperazine → 1-(4-Fluorobenzyl)-3-methylpiperazine

https://huagongshe.com/reaction/1267973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpiperazineHCID 66057—
Reactant4-Fluorobenzyl bromideHCID 68021—
SolventDichloromethaneHCID 6344—
Product1-(4-Fluorobenzyl)-3-methylpiperazineHCID 1070358412%

Reaction Steps

To a solution of 2-methylpiperazine (0.10 g, 1 mmol) in CH2Cl2 (2 mL) was added 4-fluorobenzyl bromide (0.125 mL, 1 mmol). The resultant mixture was stirred at ambient temperature. After 15 hours, the mixture was concentrated in vacuo to afford a solid. This solid was dissolved in CH2Cl2 and washed sequentially with water, aqueous NaHCO3 solution, then brine. The organic layer was dried over MgSO4, filtered, and concentrated to an oil. Purification by flash column chromatography afforded 0.025 g (12% yield) of 1-(4-fluorobenzyl)-3-methylpiperazine, a compound of formula (C), as a colorless oil; NMR (CDCl3) 7.3 (m, 2), 7.0 (m, 2), 3.4 (s, 2), 3.0-2.6 (m, 5), 2.0 (br s, 2), 1.6 (t, 1), 1.0 (d, 3) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555537B2
Source datasetuspto-grants-2003_04
ORD IDord-e78ae5f08651452a80f7d0eb4d741b23
Source noteuspto-grants-2003_04