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HRID 66655作成日:2026年10月25日

Formaldehyde → 2-(4-Carboxy-1-piperidylmethyl)propenenitrile

https://huagongshe.com/reaction/66655

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物4-Piperidinecarboxylic acidHCID 3773—
反応物Sodium ChlorideHCID 5234—
反応物Cyanoacetic acidHCID 9740—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物2-(4-Carboxy-1-piperidylmethyl)propenenitrileHCID 13037608—

反応条件

温度35 °C

反応手順

Cyanoacetic acid (12.8 g. 0.15 mole) was dissolved in 25 ml. of dioxane. Next, isonipecotic acid (19.4 g., 0.15 mole) was added. Then, 37% aqueous formaldehyde (25 g., 0.3 mole) was dripped in and the temperature maintained at a maximum of 35° C. After mixing overnight sodium chloride was added to saturation and methylene chloride used to extract the mixture. The organic phase was washed with water, dried over anhydrous sodium sulfate and after filtration, concentrated. Most of the product appeared in the aqueous phase. This was extracted twice with 500 ml. of methylene chloride in a continuous extractor. The residue obtained after solvent removal weighed 14.2 g., m.p. 109°-111° C. of analytical purity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342872
出典データセットuspto-grants-1982_08
ORD IDord-6bd5bd60a0f443a8943465267abf582a
出典メモuspto-grants-1982_08