참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2,3,4,5-Tetrahydropyridine | HCID 68161 | — |
| 반응물 | p-Laurylacetophenone | HCID 80582 | — |
| 반응물 | Dodecahydro-4H,8H,12H-4a,8a,12a-triazatriphenylene | HCID 136344 | — |
| 반응물 | Carbonic acid, monomethyl ester, magnesium salt (2:1) | HCID 167017 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4'-Dodecyl-2-(2-piperidyl)acetophenone | HCID 12300451 | 80% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03931155 |
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| 출처 데이터셋 | uspto-grants-1976_01 |
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| ORD ID | ord-18c06bb23a9f487691b80b6681a599c4 |
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| 출처 메모 | uspto-grants-1976_01 |
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