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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66651생성일: 2026년 10월 27일

Carbon Dioxide → 2-Methylpiperidine

https://huagongshe.com/reaction/66651

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물FormaldehydeHCID 712—
반응물Cyanoacetic acidHCID 9740—
반응물Piperidine, 4-(1,1-dimethylethyl)-HCID 74661—
반응물2-[(2-Methyl-1-piperidyl)methyl]propenenitrileHCID 54220988—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물2-MethylpiperidineHCID 7974—
생성물Piperidine, 4-(1,1-dimethylethyl)-HCID 74661—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04342872
출처 데이터셋uspto-grants-1982_08
ORD IDord-b90ebba6148c4c49a5ca4747826d7ecb
출처 메모uspto-grants-1982_08