戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 219053作成日:2026年10月27日

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

https://huagongshe.com/reaction/219053

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentanethiolHCID 15510—
反応物Tert-butyl[(3-iodobenzyl)oxy]dimethylsilaneHCID 66845200—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TriethylamineHCID 8471—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 6684580182.2%

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198483B2
出典データセットuspto-grants-2012_06
ORD IDord-e05832aa3012408b875354d4737b7f28
出典メモuspto-grants-2012_06