참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,3,4,5-Tetrahydropyridine | HCID 68161 | — |
| 반응물 | Carbonic acid, monomethyl ester, magnesium salt (2:1) | HCID 167017 | — |
| 반응물 | 5-Methyl-6-phenyl-3,5-hexadien-2-one | HCID 54356570 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | HCID 53954090 | HCID 53954090 | 48% |
반응 단계
Magnesium methyl carbonate (1.2 moles, 2 N in dimethylformamide) is heated to 120°C. under an atmosphere of carbon dioxide. The compound 5-methyl-6-phenyl-3,5-hexadien-2-one, 53.0 g (0.285 mole) is added and the mixture is stirred at 120°C. for a period of 4 hours under a stream of nitrogen while permitting the methanol that forms to escape. The mixture is allowed to cool under an atmosphere of carbon dioxide and 57.0 g (0.68 mole) of 2,3,4,5-tetrahydropyridine (as α-tripiperidein) is added and stirred at room temperature under an atmosphere of carbon dioxide for a period of 70 hours. The reaction mixture is poured into a concentrated HCl-ice mixture and extracted with methylene dichloride. The extracts are combined, washed with water, dried over anhydrous sodium sulfate, and the solvent removed. The crude 5-methyl-6-phenyl-1-(2-piperidyl)-3,5-hexadein-2-one which remains is recrystallized twice from isopropyl alcohol as the hydrochloride salt and is obtained in 48% yield (41.6 g) and has a M.P. of 179-80°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-fa6b7a3045384436ae45b1a518257bc9 |
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| 출처 메모 | uspto-grants-1976_01 |
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