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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78730생성일: 2026년 10월 24일

Potassium Carbonate → tert-Butyl 3-(4-bromophenylthio)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/78730

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-BromothiophenolHCID 66049—
반응물N-Boc-3-mesyloxypiperidineHCID 568122—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물tert-Butyl 3-(4-bromophenylthio)piperidine-1-carboxylateHCID 8668278518.2%

반응 단계

A mixture of 4-bromobenzenethiol (4.697 g, 24.84 mmol), tert-butyl 3-methylsulfonyloxypiperidine-1-carboxylate (6.939 g, 24.84 mmol) and K2CO3 (6.866 g, 49.68 mmol) in DMF (40 mL) were stirred at ambient temperature for 16 hours. The reaction mixture was cooled to 0° C. and diluted with water. The reaction mixture was extracted with ethylacetate (×2) and the combined organic extracts washed with saturated aqueous sodium thiosulphate solution (×2), water (×2), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 330 g eluting with 0 to 50% Et2O/Petroleum Ether, loaded in DCM) to give tert-butyl 3-((4-bromophenyl)thio)piperidine-1-carboxylate as a colourless oil (1.68 g, 18% Yield). H NMR (400.0 MHz, CDCl3) δ 0.97-0.86 (m, 2H), 1.44 (s, 9H), 1.80-1.76 (m, 1H), 2.12-2.08 (m, 1H), 2.92-2.86 (m, 1H), 3.14-3.08 (m, 2H), 3.89 (br d, 1H), 4.05 (br s, 1H), 7.30 (d, 2H) and 7.45-7.43 (m, 2H) ppm;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841449B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-be15b7c7894e4bedbaa71244c6cbea71
출처 메모uspto-grants-2014_09