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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2369715생성일: 2026년 10월 25일

Cyclopentanethiol → Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilane

https://huagongshe.com/reaction/2369715

반응식

참여 물질

역할이름HCID투입량
반응물CyclopentanethiolHCID 15510—
반응물Tert-butyl[(3-iodobenzyl)oxy]dimethylsilaneHCID 66845200—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TriethylamineHCID 8471—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 6684580182.2%

반응 단계

Tert-butyl[(3-iodobenzyl)oxy]dimethylsilane (WO9513095) (1.44 g) in dry 1-methyl-2-pyrrolidone (15 ml) and triethylamine (4 ml) was stirred at room temperature under nitrogen. 1-1′Bis(diphenylphosphino)ferrocene (110 mg) and tris(dibenzylideneacetone)dipalladium(0) (258 mg) were added and the mixture was stirred for 15 min. Cyclopentyl mercaptan (0.42 g) was then added, and the reaction mixture stirred at 60° C. for 2 h. The reaction mixture was cooled to room temperature, poured onto water and extracted with diethyl ether. The combined organic extracts were dried (MgSO4) and the solvent evaporated in vacuo. The residue was purified on a 50 g SPE, eluting with a stepped gradient of 10 to 100% dichloromethane-cyclohexane to give the title compound (1.09 g) LCMS RT=4.67 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE044874E1
출처 데이터셋uspto-grants-2014_04
ORD IDord-d75dd3502e0e460c9fe2eefae1782a8c
출처 메모uspto-grants-2014_04