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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2244042생성일: 2026년 10월 27일

Tris(propan-2-yl)silanethiol → 4-(2-Triisopropylsilanylsulfanyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2244042

반응식

참여 물질

역할이름HCID투입량
반응물Tris(propan-2-yl)silanethiolHCID 3435097—
반응물Sodium t-butoxideHCID 23676156—
반응물4-[2-(Nonafluorobutane-1-sulfonyloxy)-phenyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 86618101—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물4-(2-Triisopropylsilanylsulfanyl-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 6863578345.2%

반응 조건

온도100 °C

반응 단계

Bis[(2-diphenylphosphino)phenyl]ether (0.43 g; 0.80 mmol) and tris(dibenzylideneacetone)-dipalladium (0.37 mg; 0.40 mmol) were dissolved in 40 mL toluene. 4-[2-(Nonafluorobutane-1-sulfonyloxy)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester (4.34 g; 7.76 mmol), triisopropyl-silanethiol (1.83 mL; 8.53 mmol) and sodium tert-butoxide (0.90 g; 9.3 mmol) were added and the reaction mixture was stirred under argon for 3 hours at 100° C. The reaction mixture was cooled to room temperature filtered through a pad of silica and concentrated in vacuo. The residue was purified by flash chromatography (silica gel; ethyl acetate/heptane) to give 1.58 g 4-(2-triisopropylsilanylsulfanyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (3.51 mmol; 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07678800B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-2901406dc23346ca8309fc82d596b1fd
출처 메모uspto-grants-2010_03