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HRID 47354생성일: 2026년 10월 26일

Potassium Fluoride → 4-(1-Ethoxyvinyl)-2-fluoro-3-pyridinecarbaldehyde

https://huagongshe.com/reaction/47354

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물Stannane, tributyl(1-ethoxyethenyl)-HCID 619414—
반응물2-Fluoro-4-iodopyridine-3-carbaldehydeHCID 9992328—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물4-(1-Ethoxyvinyl)-2-fluoro-3-pyridinecarbaldehydeHCID 22745018—

반응 단계

There are mixed in succession 8 g (31.9 mmol) of 2-fluoro-4-iodo-3-pyridinecarbaldehyde (described in J.O.C, 1993, 58, pp. 7832), 12.7 g (35.96 mmol) of 1-ethoxyvinyltributyltin and 740 mg of tetrakis(triphenylphosphine)palladium (2% molar) in 280 ml of dioxane. The reaction mixture is heated at reflux until the starting material has disappeared completely. After returning to room temperature a solution of potassium fluoride is added to the reaction mixture. Vigorous stirring is maintained for 10 minutes in order to cause precipitation of the tributyltin fluoride, which is filtered off. The filtrate is plunged into a sodium chloride solution. The aqueous phase is extracted 3 times with dichloromethane and then the organic phases are combined, dried over magnesium sulphate, concentrated and purified by chromatography over a silica column, using a dichloromethane/cyclohexane mixture (95/5) as eluant to yield the expected product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699876B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-b1911e1b043043799444f39d04e81d1e
출처 메모uspto-grants-2004_03