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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 488382Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/488382

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethylpiperazineHCID 66057—
Edukt4-Fluorobenzyl bromideHCID 68021—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(4-Fluorobenzyl)-3-methylpiperazineHCID 1070358412%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06972290B2
Quelldatensatzuspto-grants-2005_12
ORD IDord-cff5b7fcab3e41c3971850bf914e8f72
Quellennotizuspto-grants-2005_12