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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379933생성일: 2026년 10월 24일

1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine → tert-Butyl 4-(acetylthio)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/379933

반응식

참여 물질

역할이름HCID투입량
반응물1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
반응물Potassium ethanethioateHCID 23670855—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물tert-Butyl 4-(acetylthio)piperidine-1-carboxylateHCID 22494773905.4%

반응 조건

온도105 °C

반응 단계

In 40 ml of dimethylformamide were dissolved 4.12 g (14.7 mmol) of 1-(tert-butoxycarbonyl)-4-(methanesulfonyloxy)piperidine, and 2.53 g (2.21 mmol) of potassium thioacetate were added to the solution, followed by stirring of the resulting mixture at 105° C. for 4 hours under nitrogen atmosphere. After cooling, the reaction mixture was diluted with ethyl acetate and washed with water and then a saturated aqueous NaCl solution, followed by evaporation of the solvent. The thus obtained residue was subjected to silica gel column chromatography and the fractions eluted with a mixed solvent of hexane-ethyl acetate (5:1) were collected to obtain 5.19 g (yield: 81%) of the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300357B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-bffff60e8d2d40cca11441a4679f6732
출처 메모uspto-grants-2001_10