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HRID 1579508생성일: 2026년 10월 27일

Carbon Dioxide → 2-Dibenzofuranyl 2-piperidylmethyl ketone

https://huagongshe.com/reaction/1579508

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물2,3,4,5-TetrahydropyridineHCID 68161—
반응물Carbonic acid, monomethyl ester, magnesium salt (2:1)HCID 167017—
반응물2-AcetyldibenzofuranHCID 293028—
용매MethanolHCID 887—
생성물2-Dibenzofuranyl 2-piperidylmethyl ketoneHCID 1230050732%

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03931155
출처 데이터셋uspto-grants-1976_01
ORD IDord-01651cfff3bb4c8482ebafc4ee0219f3
출처 메모uspto-grants-1976_01