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HRID 65743생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물AziridineHCID 9033—
반응물5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
용매TetrahydrofuranHCID 8028—
생성물2-[[5-(Dimethylamino)methyl-2-furanyl]methoxy]ethanamineHCID 202133122.5%

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04128658
출처 데이터셋uspto-grants-1978_12
ORD IDord-455eb8b5e01d44359c3ecf6e15714f60
출처 메모uspto-grants-1978_12