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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336836Erstellt: 24. Oktober 2026

1-Methylpiperazine → 5-((4-Methylpiperazine-1-yl)methyl)furan-2-carboxaldehyde

https://huagongshe.com/de/reaction/336836

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylpiperazineHCID 53167—
Edukt5-(Bromomethyl)-2-furaldehydeHCID 11970491—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-((4-Methylpiperazine-1-yl)methyl)furan-2-carboxaldehydeHCID 8667138155%

Reaktionsschritte

To a solution of 0.20 g (1.1 mmol) of 5-(bromomethyl)furan-2-carboxaldehyde in anhydrous dioxane (10 ml) are added 261 μL (0.24 g, 2.3 mmol) of 1-methylpiperazine. The mixture is stirred at room temperature for 30 min. The precipitate formed is filtered and rinsed with dioxane. The filtrate is concentrated, dissolved in dichloromethane, and washed in water. The organic phase is dried over magnesium sulfate, filtered, and concentrated. The residue obtained is purified by chromatography on silica (eluent: 7N NH4OH in MeOH/CH2Cl2, 5:95) to yield 0.12 g (55%) of 5-((4-methylpiperazine-1-yl)methyl)furan-2-carboxaldehyde in the form of an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889711B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-c4556eb69876429c80231218238a6038
Quellennotizuspto-grants-2014_11