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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1505869생성일: 2026년 10월 26일

Iodine → 1-[1-(4-Bromophenyl)-1-methyl-ethyl]-piperidine

https://huagongshe.com/reaction/1505869

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물1,4-DibromobenzeneHCID 7804—
반응물Potassium CarbonateHCID 11430—
반응물2-Methyl-2-piperidin-1-ylpropanenitrileHCID 288882—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-[1-(4-Bromophenyl)-1-methyl-ethyl]-piperidineHCID 5826638695%

반응 단계

In a three necked round bottom flask fitted with a condenser and nitrogen stream, was placed a small quantity of ground glass and magnesium turnings (190 mg, 7.40 mmol). The mixture was stirred for 30 minutes under vacuum then placed under nitrogen and iodine added (one small crystal), followed by the rapid addition of 1,4-dibromobenzene (2.43 g, 10.3 mmol) in 15 ml of anhydrous diethyl ether. The reaction mixture was then heated under reflux for 5 minutes. After this time, a solution of 1-(1-cyano-1-methylethyl)-piperidine (1.0 g, 6.60 mmol) in anhydrous THF was added dropwise resulting in the formation of a white precipitate. The reaction mixture was heated under reflux for 1.5 h, before cooling to ambient temperature. The resultant mixture was treated with saturated aqueous potassium carbonate solution and extracted with DCM. The organic extract was dried over magnesium sulfate and concentrated in vacuo. The crude residue was purified by column chromatography (silica, 12 g column, ISCO, 0-40% ethyl acetate in cyclohexane) to afford the title compound (200 mg, 95%) as a colourless oil. LCMS (Method B): RT=1.99 min, M+H+=282, 284.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09216980B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-9a101a81e3ba419d999350151f6f6393
출처 메모uspto-grants-2015_12