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HRID 47354作成日:2026年10月26日

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

https://huagongshe.com/reaction/47354

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium FluorideHCID 522689—
反応物Stannane, tributyl(1-ethoxyethenyl)-HCID 619414—
反応物2-Fluoro-4-iodopyridine-3-carbaldehydeHCID 9992328—
触媒HCID 178418397HCID 178418397—
溶媒1,4-DioxaneHCID 31275—
生成物4-(1-Ethoxyvinyl)-2-fluoro-3-pyridinecarbaldehydeHCID 22745018—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699876B2
出典データセットuspto-grants-2004_03
ORD IDord-b1911e1b043043799444f39d04e81d1e
出典メモuspto-grants-2004_03