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HRID 23701作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物AcetonitrileHCID 6342—
反応物3-FuraldehydeHCID 10351—
反応物Potassium HydroxideHCID 14797—
反応物Trimethylsulfonium iodideHCID 75127—
生成物1-(Furan-3-yl)-2-(methylamino)ethan-1-olHCID 1028580319%

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852731B2
出典データセットuspto-grants-2005_02
ORD IDord-3f3c04bad60e414b8dc66d5d8769618c
出典メモuspto-grants-2005_02