化工社化工社 化学情報印刷レポート · 研究参考用
Tetrabutylammonium Fluoride → [3-(Cyclopentylsulfanyl)phenyl]methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 反応物 | Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilane | HCID 66845801 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [3-(Cyclopentylsulfanyl)phenyl]methanol | HCID 66347770 | 92.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07361787B2 |
| 出典データセット | uspto-grants-2008_04 |
| ORD ID | ord-76117cad6b9640ef8967ae979cdfa5dc |
| 出典メモ | uspto-grants-2008_04 |