戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 901632作成日:2026年10月26日

Tetrabutylammonium Fluoride → [3-(Cyclopentylsulfanyl)phenyl]methanol

https://huagongshe.com/reaction/901632

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneHCID 66845801—
溶媒TetrahydrofuranHCID 8028—
生成物[3-(Cyclopentylsulfanyl)phenyl]methanolHCID 6634777092.3%

反応手順

A solution of tetrabutylammonium fluoride in THF (1M, 6 ml) was added to a solution of tert-butyl{[3-(cyclopentylthio)benzyl]oxy}dimethylsilane (1.09 g) in dry THF (10 ml). The solution was stirred for 18 h under nitrogen and the solvent was evaporated in vacuo. The residue was partitioned between dichloromethane and water. The organic phase was separated and washed with water. The organic phase was separated and the solvent evaporated in vacuo. The residue was purified on a 10 g silica SPE cartridge, eluting with a stepped gradient of 10% to 100% dichloromethane-cyclohexane to give the title compound (0.65 g). LCMS RT=3.3 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361787B2
出典データセットuspto-grants-2008_04
ORD IDord-76117cad6b9640ef8967ae979cdfa5dc
出典メモuspto-grants-2008_04