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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219053Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/219053

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopentanethiolHCID 15510—
EduktTert-butyl[(3-iodobenzyl)oxy]dimethylsilaneHCID 66845200—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktTert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 6684580182,2%

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198483B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-e05832aa3012408b875354d4737b7f28
Quellennotizuspto-grants-2012_06