참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Cyanoacetic acid | HCID 9740 | — |
| 반응물 | Piperidine, 4-(1,1-dimethylethyl)- | HCID 74661 | — |
| 반응물 | 2-[(2-Methyl-1-piperidyl)methyl]propenenitrile | HCID 54220988 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2-Methylpiperidine | HCID 7974 | — |
| 생성물 | Piperidine, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04342872 |
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| 출처 데이터셋 | uspto-grants-1982_08 |
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| ORD ID | ord-b90ebba6148c4c49a5ca4747826d7ecb |
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| 출처 메모 | uspto-grants-1982_08 |
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