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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23701Erstellt: 23. Oktober 2026

Water → 1-(Furan-3-yl)-2-(methylamino)ethan-1-ol

https://huagongshe.com/de/reaction/23701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAcetonitrileHCID 6342—
Edukt3-FuraldehydeHCID 10351—
EduktPotassium HydroxideHCID 14797—
EduktTrimethylsulfonium iodideHCID 75127—
Produkt1-(Furan-3-yl)-2-(methylamino)ethan-1-olHCID 1028580319%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

Trimethylsulfonium iodide (20.4 g) and 3-furaldehyde (8.65 mL) are added to potassium hydroxide (11.2 g) and H2O (0.45 mL) in acetonitrile (150 mL). The reaction mixture is heated to 60° C. for 2.5 h. The reaction mixture is allowed to cool to room temperature. The precipitate is filtered off, and the filtrate is concentrated in vacuo. The resulting crude epoxide (10.747 g) is dissolved in methanol (50 mL) and added to a 2.0 M solution of methylamine in methanol (100 mL). The reaction mixture is stirred at room temperature for 3 d and then heated to reflux for 30 min. The reaction mixture is allowed to cool to room temperature and is concentrated in vacuo. The resulting brown oil was purified via column chromatography (CHCl3/methanol, 95/5, 90/10; CHCl3/methanol/NH4OH, 90/10/1) to yield 2.703 g (19%) of the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-3f3c04bad60e414b8dc66d5d8769618c
Quellennotizuspto-grants-2005_02