関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl Acrylate | HCID 7294 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | 2-Bromo-3-benzyloxy-6-hydroxymethylpyridine | HCID 19692713 | — |
| 触媒 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methyl (3-benzyloxy-6-hydroxymethylpyridin-2-yl)propenoate | HCID 86751043 | 84.1% |
反応手順
To a solution of 2-bromo-3-benzyloxy-6-hydroxymethylpyridine (2.94 g, 10 mmol) in DMF (19 ml) and water (1 ml) were added potassium acetate (2.45 g, 10.0 mmol), tetra-n-butylammonium iodide (3.69 g. 10.0 mmol), bis(triphenyl-phosphine)palladium dichloride (281 mg, 0.4 mmol) and methyl acrylate (2.70 ml. 2.58 g, 30 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 5 h. The mixture was cooled and added to water (180 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (3×25 ml), dried and evaporated. The residue was purified by flash column chromatography eluting with dichloromethane, then 4:1 dichloromethane:ethyl acetate to give the product (2.516 g, 84%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05726315 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-a748f251ca1d423aa7e17eaf3d09ac7f |
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| 出典メモ | uspto-grants-1998_03 |
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