関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| 反応物 | 2-Fluoro-4-iodopyridine-3-carbaldehyde | HCID 9992328 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 4-(1-Ethoxyvinyl)-2-fluoro-3-pyridinecarbaldehyde | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06699876B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-b1911e1b043043799444f39d04e81d1e |
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| 出典メモ | uspto-grants-2004_03 |
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