Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Piperidine, 4-(1,1-dimethylethyl)- | HCID 74661 | — |
| Reactant | 2-[(2-Methyl-1-piperidyl)methyl]propenenitrile | HCID 54220988 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Methylpiperidine | HCID 7974 | — |
| Product | Piperidine, 4-(1,1-dimethylethyl)- | HCID 74661 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04342872 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-b90ebba6148c4c49a5ca4747826d7ecb |
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| Source note | uspto-grants-1982_08 |
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