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Water → {3-[(4-Bromophenyl)sulfanyl]propoxy}(tert-butyl)dimethylsilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Bromothiophenol | HCID 66049 | — |
| 反応物 | (3-Bromopropoxy)(tert-butyl)dimethylsilane | HCID 607486 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | {3-[(4-Bromophenyl)sulfanyl]propoxy}(tert-butyl)dimethylsilane | HCID 58452783 | 95.9% |
反応手順
Potassium carbonate (4.1 g) and (3-bromopropoxy)-tert-butyldimethylsilane (4.1 g) were added to a solution of 4-bromothiophenol (3.0 g) in N,N-dimethylformamide, and the mixture was stirred at room temperature overnight. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:1→20:1) to give the title compound as a colorless oil (5.5 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08822503B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-89f6114bf4d848c3aab847590a690aff |
| 出典メモ | uspto-grants-2014_09 |