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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23701생성일: 2026년 10월 23일

Water → 1-(Furan-3-yl)-2-(methylamino)ethan-1-ol

https://huagongshe.com/ko/reaction/23701

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcetonitrileHCID 6342—
반응물3-FuraldehydeHCID 10351—
반응물Potassium HydroxideHCID 14797—
반응물Trimethylsulfonium iodideHCID 75127—
생성물1-(Furan-3-yl)-2-(methylamino)ethan-1-olHCID 1028580319%

반응 조건

온도60 °C

반응 단계

Trimethylsulfonium iodide (20.4 g) and 3-furaldehyde (8.65 mL) are added to potassium hydroxide (11.2 g) and H2O (0.45 mL) in acetonitrile (150 mL). The reaction mixture is heated to 60° C. for 2.5 h. The reaction mixture is allowed to cool to room temperature. The precipitate is filtered off, and the filtrate is concentrated in vacuo. The resulting crude epoxide (10.747 g) is dissolved in methanol (50 mL) and added to a 2.0 M solution of methylamine in methanol (100 mL). The reaction mixture is stirred at room temperature for 3 d and then heated to reflux for 30 min. The reaction mixture is allowed to cool to room temperature and is concentrated in vacuo. The resulting brown oil was purified via column chromatography (CHCl3/methanol, 95/5, 90/10; CHCl3/methanol/NH4OH, 90/10/1) to yield 2.703 g (19%) of the title compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-3f3c04bad60e414b8dc66d5d8769618c
출처 메모uspto-grants-2005_02