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HRID 126837作成日:2026年10月27日

Carbon Dioxide → 2-(4-Fluoro-1-piperidylmethyl)propenenitrile

https://huagongshe.com/reaction/126837

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物FormaldehydeHCID 712—
反応物Cyanoacetic acidHCID 9740—
反応物Sodium BicarbonateHCID 516892—
反応物4-FluoropiperidineHCID 2759159—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物2-(4-Fluoro-1-piperidylmethyl)propenenitrileHCID 13041034—

反応条件

温度65 °C

反応手順

4-Fluoropiperidine (0.7 g., 0.005 mole) was dissolved in a mixture of 3 ml. of dioxane and 2 ml. of water containing cyanoacetic acid (0.43 g., 0.005 mole). Then, 0.85 g. (0.01 mole) of 37% aqueous formaldehyde was added to the solution. The solution was heated to 65° C. and carbon dioxide evolution began. It was maintained at 60°-65° C. for 21/2 hours and allowed to stand overnight. A solid gummy residue, 1 gm., was obtained upon stripping in a bath at 55° C. and at 1 mm. It was taken up in a small amount of water, made alkaline with sodium bicarbonate and extracted with ether. The organic layer was water washed and dried over anhydrous sodium sulfate. After solvent stripping, the product was obtained as a colorless oil, 0.7 g., of analytical purity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254131
出典データセットuspto-grants-1981_03
ORD IDord-bbf5626a65f8497384b49ee61d97e8ac
出典メモuspto-grants-1981_03