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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55264생성일: 2026년 10월 24일

(Z)-1-Ethoxy-2-(tributylstannyl)ethene → 6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester

https://huagongshe.com/ko/reaction/55264

반응식

참여 물질

역할이름HCID투입량
반응물(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
반응물6-iodo-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl esterHCID 86750765—
용매TolueneHCID 1140—
생성물6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl esterHCID 8675076423.1%

반응 조건

온도110 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624943
출처 데이터셋uspto-grants-1997_04
ORD IDord-5374a5b7c4d54206b10cb491f614f631
출처 메모uspto-grants-1997_04