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HRID 391730생성일: 2026년 10월 24일

Tri(butyl)vinyltin → 1-(2-Methoxy-4-nitrophenyl)-3-vinylpyridin-2(1H)-one

https://huagongshe.com/ko/reaction/391730

반응식

참여 물질

역할이름HCID투입량
반응물Tri(butyl)vinyltinHCID 53438229—
반응물3-Bromo-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-oneHCID 59410145—
용매1,4-DioxaneHCID 31275—
생성물1-(2-Methoxy-4-nitrophenyl)-3-vinylpyridin-2(1H)-oneHCID 59410176—

반응 단계

100 g (308 mmol) of the compound from Example 19A are dissolved in 1.4 l of anhydrous dioxane, and 8.9 g (7.7 mmol) of tetrakis(triphenylphospine)palladium and 117 g (370 mmol) of tributylvinyltin are added. The mixture is heated at reflux for 16 h. The reaction solution is then allowed to cool and filtered through kieselguhr. The filtrates are concentrated to dryness under reduced pressure. The residue is chromatographed on silica gel using a gradient of cyclohexane and ethyl acetate. The product-containing fractions are combined and concentrated to dryness under reduced pressure. Petroleum ether is added until crystallization sets in. The crystals are filtered off and dried under reduced pressure. This gives 37 g (41% of theory) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383822B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-b2766cb001604a1f9e6dc43f63304cbc
출처 메모uspto-grants-2013_02