関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Methyl Acrylate | HCID 7294 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-Benzyloxy-2-iodopyridine | HCID 19957501 | — |
| 触媒 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (E)-Methyl 3-[3-(phenylmethoxy)pyridin-2-yl]-2-propenoate | HCID 22161738 | — |
反応手順
5.2 g of palladium(II) acetate, 77.8 g of potassium carbonate and 72.5 g of tetrabutylammonium bromide are added to a solution of 70 g of 3-benzyloxy-2-iodopyridine and 39.8 ml of acrylic acid methyl ester in 120 ml of dimethylformamide, and the suspension is stirred under argon atmosphere for 10 hours at 100° C. (bath temperature). The reaction mixture is concentrated by evaporation in a vacuum, the residue is added to water and shaken out with ethyl acetate. The organic phase is washed three times with water and once with saturated common salt solution, dried with sodium sulfate and concentrated by evaporation. The crude product is chromatographed on silica gel with hexane/10-25% ethyl acetate. 48.2 g of 3-(3-benzyloxy-2-pyridyl)-(2E)-2-propenoic acid methyl ester is obtained as oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05624943 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-d4846378d04a4d3fb9385b65082d0c14 |
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| 出典メモ | uspto-grants-1997_04 |
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