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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127308생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/127308

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, 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255440
출처 데이터셋uspto-grants-1981_03
ORD IDord-c0326498108841bcbece3248ebb4d258
출처 메모uspto-grants-1981_03