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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369715Generated: October 25, 2026

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

https://huagongshe.com/reaction/2369715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanethiolHCID 15510—
ReactantTert-butyl[(3-iodobenzyl)oxy]dimethylsilaneHCID 66845200—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTriethylamineHCID 8471—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductTert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 6684580182.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE044874E1
Source datasetuspto-grants-2014_04
ORD IDord-d75dd3502e0e460c9fe2eefae1782a8c
Source noteuspto-grants-2014_04