参与物
| 角色 | 名称 | HCID | 投料 |
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| 反应物 | Carbonic acid sodium salt (1:2) | HCID 10340 | — |
| 反应物 | 碳酸钾 | HCID 11430 | — |
| 反应物 | N-溴代丁二酰亚胺(NBS) | HCID 67184 | — |
| 反应物 | (2-氯吡啶-4-基)甲醇 | HCID 7062237 | — |
| 溶剂 | 乙酸乙酯 | HCID 8857 | — |
| 产物 | 2-氯吡啶-4-甲醛 | HCID 2762994 | — |
反应步骤
A suspension of 2-chloro-4-pyridinemethanol (8.0 g, 55.9 mmol), NBS (14.9 g, 83.9 mmol), and K2CO3 (11.75 g, 97.1 mmol) in EtOAc was refluxed for 3 h. A second portion of NBS (14.9 g, 83.9 mmol) and Na2CO3 (12.0 g, 114 mmol) were added and the reaction was heated to reflux for an additional 3.5 h, cooled and filtered through a pad of celite. The filtrate, after concentrattion to a small volume, was subjected to flash chromatography eluting with 0.5-4% CH3OH/CH2Cl2. The fractions containing product were combined, washed successively with sat aq NaHCO3 10% Na2S2O3, and brine, dried (MgSO4) and concentrated in vacuo to give the title compound as a light yellow solid; yield 5.3 g (67%). 1H NMR (CDCl3) δ10.06 (s, 1H), 8.66 (d, 1H, J=5.0 Hz), 7.76 (s, 1H), 7.66 (d, 1H, J=5.0 Hz).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US06218537B1 |
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| 来源数据集 | uspto-grants-2001_04 |
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| ORD ID | ord-bb2021ce32a34a9d83b9e17c7efcd92c |
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| 来源说明 | uspto-grants-2001_04 |
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