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HRID 66661作成日:2026年10月26日

Carbon Dioxide → 2-Methylpiperidine

https://huagongshe.com/reaction/66661

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Piperidine, 4-(1,1-dimethylethyl)-HCID 74661—
反応物2-[(2-Methyl-1-piperidyl)methyl]propenenitrileHCID 54220988—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物2-MethylpiperidineHCID 7974—
生成物Piperidine, 4-(1,1-dimethylethyl)-HCID 74661—

反応手順

Cyanoacetic acid (1.75 g., 0.02 mole) was dissolved in 10 ml. of dioxane. In a five minute period 4-t-butylpiperidine (2.8 g., 0.02 mole) was added, the temperature rose to 25° C. from 15° C. obtained by prior cooling with an ice bath. The mixture which solidified became fluid upon the addition of 37% aqueous formaldehyde (3.6 g., 0.04 mole), the temperature rose to 30° C. and carbon dioxide evolution began. The mixture was stirred an additional 12 hours, was taken up in ether and the organic phase separated and washed with water. The dried ether solution was stripped of solvent to leave a solid residue product, 3.7 g. of practically analytical purity. In place of 4-t-butylpiperidine, the use of 2-methylpiperidine (0.02 mole) provided 2-[(2-methyl-1-piperidyl)methyl]propenenitrile as a colorless oil, RfSiO2 0.58 (5% ethanol in methylene chloride).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342873
出典データセットuspto-grants-1982_08
ORD IDord-d13f047e567d4584a1e912b652a71883
出典メモuspto-grants-1982_08