Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3,4,5-Tetrahydropyridine | HCID 68161 | — |
| Reactant | p-Laurylacetophenone | HCID 80582 | — |
| Reactant | Dodecahydro-4H,8H,12H-4a,8a,12a-triazatriphenylene | HCID 136344 | — |
| Reactant | Carbonic acid, monomethyl ester, magnesium salt (2:1) | HCID 167017 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12300451 | HCID 12300451 | 80% |
Reaction Steps
Magnesium methyl carbonate (0.5 mole 1 M in dimethylformamide) is heated to 120°C. under an atmosphere of carbon dioxide. The compound 4'-dodecylacetophenone, 28.9 g (0.1 mole), is added, and the mixture stirred at 120°C. for 4 hours under a stream of nitrogen, allowing the methanol that forms to escape. The reaction mixture is cooled to room temperature under an atmosphere of carbon dioxide and 10.1 g (0.12 mole) of 2,3,4,5-tetrahydropyridine trimer (α-tripiperidein) is added. The mixture is stirred at room temperature for 66 hours in an atmosphere of carbon dioxide and poured into a solution 800 ml of 2N HCl. The solid is removed by filtration, dissolved in methylene dichloride, dried over anhydrous sodium sulfate and azeotroped with methyl ether until the product precipitates. The 4'-dodecyl-2-(2-piperidyl)acetophenone, when recrystallized as the hydrochloride salt from a methylene dichloride-ethyl ether mixture, is obtained in 80% yield, (32.5 g) and has a M.P. of 126-7°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931155 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-18c06bb23a9f487691b80b6681a599c4 |
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| Source note | uspto-grants-1976_01 |
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