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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65743Generated: October 26, 2026

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

https://huagongshe.com/reaction/65743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantAziridineHCID 9033—
Reactant5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
SolventTetrahydrofuranHCID 8028—
Product2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamineHCID 202133122.5%

Reaction Steps

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, 5N 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. Route (ii)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128658
Source datasetuspto-grants-1978_12
ORD IDord-455eb8b5e01d44359c3ecf6e15714f60
Source noteuspto-grants-1978_12