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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

反応式

関与物質

役割名称HCID仕込み量
反応物(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
反応物6-iodo-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl esterHCID 86750765—
溶媒TolueneHCID 1140—
生成物6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl esterHCID 8675076423.1%

反応条件

温度110 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624943
出典データセットuspto-grants-1997_04
ORD IDord-5374a5b7c4d54206b10cb491f614f631
出典メモuspto-grants-1997_04