HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65743Generated: October 27, 2026
Methanesulfonic Acid → 2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamine
https://huagongshe.com/reaction/65743
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Aziridine | HCID 9033 | — |
| Reactant | 5-((Dimethylamino)methyl)-2-furanmethanol | HCID 84906 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamine | HCID 20213312 | 2.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04128658 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-455eb8b5e01d44359c3ecf6e15714f60 |
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| Source note | uspto-grants-1978_12 |
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