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 | Carbonic acid, monomethyl ester, magnesium salt (2:1) | HCID 167017 | — |
| 반응물 | 2-Acetyldibenzofuran | HCID 293028 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-Dibenzofuranyl 2-piperidylmethyl ketone | HCID 12300507 | 32% |
반응 단계
Magnesium methyl carbonate (0.6 mole, 2.5 N in dimethylformamide) is heated to 120°C. under an atmosphere of carbon dioxide. The compound 2-acetyldibenzofuran, 31.5 g (0.15 mole) is added and the mixture is stirred at 120°C. for a period of 4 hours under a stream of nitrogen to form the chelate, allowing the methyl alcohol that forms to escape. The mixture is cooled to room temperature under an atmosphere of carbon dioxide and 15.2 g (0.18 mole) of 2,3,4,5-tetrahydropyridine (as α-tripiperidine) is added and the mixture stirred at room temperature for a period of 40 hours in an atmosphere of carbon dioxide. The resulting mixture is poured into 200 ml of concentrated HCl on 600 g of ice. After standing for 48 hours the precipitate which forms is filtered and washed with ethyl ether. The 2-dibenzofuranyl-2-piperidylmethyl ketone so prepared is twice recrystallized from isopropyl alcohol as the hydrochloride salt and is obtained in 32% yield (16.0 g) and has a M.P. of 218-20°C. (dec.)
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-01651cfff3bb4c8482ebafc4ee0219f3 |
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| 출처 메모 | uspto-grants-1976_01 |
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