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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1579503생성일: 2026년 10월 27일

Carbon Dioxide → 4'-Dodecyl-2-(2-piperidyl)acetophenone

https://huagongshe.com/reaction/1579503

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물2,3,4,5-TetrahydropyridineHCID 68161—
반응물p-LaurylacetophenoneHCID 80582—
반응물Dodecahydro-4H,8H,12H-4a,8a,12a-triazatriphenyleneHCID 136344—
반응물Carbonic acid, monomethyl ester, magnesium salt (2:1)HCID 167017—
용매MethanolHCID 887—
생성물4'-Dodecyl-2-(2-piperidyl)acetophenoneHCID 1230045180%

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03931155
출처 데이터셋uspto-grants-1976_01
ORD IDord-18c06bb23a9f487691b80b6681a599c4
출처 메모uspto-grants-1976_01