참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methoxybenzyl alcohol | HCID 7738 | — |
| 반응물 | Aluminum | HCID 5359268 | — |
| 반응물 | 3-Bromo-5-(bromomethyl)-2-fluoropyridine | HCID 59548244 | — |
| 촉매 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 촉매 | HCID 178418778 | HCID 178418778 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-Bromo-2-fluoro-5-((4-methoxybenzyloxy)methyl)pyridine | HCID 59548291 | 24% |
반응 단계
3-Bromo-5-(bromomethyl)-2-fluoropyridine (5.63 g, 20.9 mmol) was dissolved in MeCN (135 mL) and 4-methoxybenzyl alcohol (5.20 mL, 41.9 mmol), silver (I) oxide (7.169 g, 30.9 mmol), and tetrabutylammonium iodide (2.208 g, 5.98 mmol) were added. The reaction flask was covered with aluminum foil and the reaction was stirred under nitrogen at room temperature overnight. The reaction was filtered through a pad of Celite® (diatomaceous earth), washing with DCM, MeOH and MeCN. The filtrate was concentrated and purified on a silica gel column (3:1 to 2:1 to 3:2 hexanes/DCM to 3:2 DCM/hexanes to 2:1 DCM/hexanes to 3:1 DCM/hexanes to DCM) to give 3-Bromo-2-fluoro-5-((4-methoxybenzyloxy)methyl)pyridine (1.62 g, 24%). MS (ESI pos. ion) m/z 326/328 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08772480B2 |
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| 출처 데이터셋 | uspto-grants-2014_07 |
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| ORD ID | ord-ab5a002a5d574e6f8c2231af6515db9c |
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| 출처 메모 | uspto-grants-2014_07 |
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