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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369716Generated: October 30, 2026

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

https://huagongshe.com/reaction/2369716

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 numberUSRE044874E1
Source datasetuspto-grants-2014_04
ORD IDord-bc4f356257c045eab18350abeae6729f
Source noteuspto-grants-2014_04