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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127308Erstellt: 25. Oktober 2026

Methanesulfonic Acid → 2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamine

https://huagongshe.com/reaction/127308

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
EduktAziridineHCID 9033—
Edukt5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamineHCID 202133122,5%

Reaktionsschritte

To a solution of 5-(dimethylamino)methyl-2-furanmethanol (6.2 g) and ethylene imine (2.82 g) in dry tetrahydrofuran was added a solution of methanesulphonic acid (11.6 g) in tetrahydrofuran (40 ml). The solution was evaporated and the oily residue heated at 98°-100° for 10 mins. After 18 hr, 5 N sodium hydroxide (60 ml) was added and the solution evaporated to dryness. Anhydrous sodium sulphate and ethyl acetate (150 ml) were added and after 2 hr the suspension was filtered, treated with decolourising charcoal and evaporated. The resulting oil was chromatographed on silica, firstly with methanol-ammonia 0.88 79:1, and the eluate discarded, and secondly with methanol-ammonia 0.88 19:1. This eluate was evaporated to give an oil from which the bisoxalate salt of 2-[[5-(dimethylamino)methyl-2-furanyl]methoxy]ethanamine (from ethanol) 0.2 g, m.p. 125°-128°, was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04255440
Quelldatensatzuspto-grants-1981_03
ORD IDord-c0326498108841bcbece3248ebb4d258
Quellennotizuspto-grants-1981_03