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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219054생성일: 2026년 10월 26일

Tetrabutylammonium Fluoride → [3-(Cyclopentylsulfanyl)phenyl]methanol

https://huagongshe.com/reaction/219054

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 66845801—
용매TetrahydrofuranHCID 8028—
생성물[3-(Cyclopentylsulfanyl)phenyl]methanolHCID 6634777092.3%

반응 단계

A solution of tetrabutylammonium fluoride in THF (1 M, 6 ml) was added to a solution of tert-butyl{[3-(cyclopentylthio)benzyl]oxy}dimethylsilane (1.09 g) in dry THF (10 ml). The solution was stirred for 18 h under nitrogen and the solvent was evaporated in vacuo. The residue was partitioned between dichloromethane and water. The organic phase was separated and washed with water. The organic phase was separated and the solvent evaporated in vacuo. The residue was purified on a 10 g silica SPE cartridge, eluting with a stepped gradient of 10% to 100% dichloromethane-cyclohexane to give the title compound (0.65 g). LCMS RT=3.3 min

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198483B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-67cf010eb7994bbd8a6ee54bc9903c72
출처 메모uspto-grants-2012_06