참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | 3-Furaldehyde | HCID 10351 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Trimethylsulfonium iodide | HCID 75127 | — |
| 생성물 | 1-(Furan-3-yl)-2-(methylamino)ethan-1-ol | HCID 10285803 | 19% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06852731B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-3f3c04bad60e414b8dc66d5d8769618c |
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| 출처 메모 | uspto-grants-2005_02 |
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