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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503095Generated: October 25, 2026

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

https://huagongshe.com/reaction/503095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantTert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 66845801—
SolventTetrahydrofuranHCID 8028—
Product[3-(Cyclopentylsulfanyl)phenyl]methanolHCID 6634777092.3%

Reaction Steps

A solution of tetrabutylammonium fluoride in THF (1M, 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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776895B2
Source datasetuspto-grants-2010_08
ORD IDord-a1f2079fea3b4810a81ee2e023de351d
Source noteuspto-grants-2010_08