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HRID 55264作成日:2026年10月25日
(Z)-1-Ethoxy-2-(tributylstannyl)ethene → 6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester
https://huagongshe.com/reaction/55264
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (Z)-1-Ethoxy-2-(tributylstannyl)ethene | HCID 2763294 | — |
| 反応物 | 6-iodo-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester | HCID 86750765 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester | HCID 86750764 | 23.1% |
反応手順
A solution of 495 mg of 3-{6-iodo-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester and 397 mg of ethoxyvinyltributyltin in 2 ml of toluene is mixed with 30 mg of bis-triphenylphosphine-palladium(II) chloride and heated for six hours with stirring to 110° C. The reaction mixture is filtered on diatomaceous earth, the filter residue is washed with diethyl ether, the filtrate is mixed with 1.5 ml of 2n hydrochloric acid and stirred for 4 hours at room temperature. The organic phase is separated, dried with sodium sulfate and concentrated by evaporation. 95 mg of 3-{6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic 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-5374a5b7c4d54206b10cb491f614f631 |
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| 出典メモ | uspto-grants-1997_04 |
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