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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85206생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/85206

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 번호US08846934B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ebcb7e09364e401d89b7b6c5f5b81626
출처 메모uspto-grants-2014_09