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HRID 2369715作成日:2026年10月26日

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

https://huagongshe.com/reaction/2369715

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USRE044874E1
出典データセットuspto-grants-2014_04
ORD IDord-d75dd3502e0e460c9fe2eefae1782a8c
出典メモuspto-grants-2014_04