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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368196Generated: October 31, 2026

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

https://huagongshe.com/reaction/1368196

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 numberUS06573266B1
Source datasetuspto-grants-2003_06
ORD IDord-782d2083b3684e3f912766547376aeba
Source noteuspto-grants-2003_06