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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1643457생성일: 2026년 10월 27일

Piperidin-2-ylmethanol → [1-(4-Methoxy-2,6-dimethyl-phenylsulfonyl)-piperidin-2-yl]-methanol

https://huagongshe.com/reaction/1643457

반응식

참여 물질

역할이름HCID투입량
반응물Piperidin-2-ylmethanolHCID 94263—
반응물Perfluorophenyl 4-methoxy-2,6-dimethylbenzenesulfonateHCID 59746536—
촉매Tetrabutylammonium ChlorideHCID 70681—
용매DimethylformamideHCID 6228—
생성물[1-(4-Methoxy-2,6-dimethyl-phenylsulfonyl)-piperidin-2-yl]-methanolHCID 43574491—

반응 조건

온도110 °C

반응 단계

Perfluorophenyl 4-methoxy-2,6-dimethylbenzenesulfonate (1 g, 2.616 mmol), 2-(hydroxymethyl)-piperidine (1.61 g, 13.079 mmol) and tetrabutylammonium chloride (1.45 g, 5.231 mmol) were dissolved in N,N-dimethylformamide (10 ml) and the solution was stirred at 110° C. for 1 h. The solvent was removed in vacuo, the residue was dissolved in ethyl acetate and the solution was washed with ammonium chloride solution (10%, 20 ml), dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica gel) with diethyl ether/hexane/methylene chloride (1:1:1). Yield: 0.63 g (76%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08119805B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-f06854afd3cf4fe5846e8e0bf8757fd8
출처 메모uspto-grants-2012_02