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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503094Generated: October 25, 2026

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

https://huagongshe.com/reaction/503094

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 numberUS07776895B2
Source datasetuspto-grants-2010_08
ORD IDord-3c1d0c72c83c4f92ade1122c2fd59647
Source noteuspto-grants-2010_08