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HRID 65743作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/65743

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物AziridineHCID 9033—
反応物5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
溶媒TetrahydrofuranHCID 8028—
生成物2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamineHCID 202133122.5%

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04128658
出典データセットuspto-grants-1978_12
ORD IDord-455eb8b5e01d44359c3ecf6e15714f60
出典メモuspto-grants-1978_12