반응식
C(=O)([O-])OC.[Mg+2].COC(=O)[O-].[CH2:12]([C:24]1[CH:29]=[CH:28][C:27]([C:30](=[O:32])[CH3:31])=[CH:26][CH:25]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].[N:33]1[CH2:34][CH2:35][CH2:36][CH2:37][CH:38]=1.C1CC2N(C3N(C4N2CCCC4)CCCC3)CC1.C(=O)=O.Cl>CO>[CH2:12]([C:24]1[CH:25]=[CH:26][C:27]([C:30](=[O:32])[CH2:31][CH:38]2[CH2:37][CH2:36][CH2:35][CH2:34][NH:33]2)=[CH:28][CH:29]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]참가 물질
반응물 6
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 120 °C
실험 절차
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.
후처리
- temperatureThe reaction mixture is cooled to room temperature under an atmosphere of carbon dioxide
- customThe solid is removed by filtration
- dissolutiondissolved in methylene dichloride
- dry with materialdried over anhydrous sodium sulfate
- customazeotroped with methyl ether until the product
- customprecipitates
- customThe 4'-dodecyl-2-(2-piperidyl)acetophenone, when recrystallized as the hydrochloride salt from a methylene dichloride-ethyl ether mixture
- customis obtained in 80% yield, (32.5 g)
출처 및 근거
- ORD 기록
- ord-18c06bb23a9f487691b80b6681a599c4
- 출처 데이터셋
- uspto-grants-1976_01
- 특허 번호
- US03931155
연결된 노트
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