関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,1',1''-(Chlorosilylidyne)tris(benzene) | HCID 6458 | — |
| 反応物 | 2-Methoxynaphthalene | HCID 7119 | — |
| 反応物 | Hexamethylphosphoramide | HCID 12679 | — |
| 反応物 | Cyclohexane hexane | HCID 22494920 | — |
| 反応物 | CID 53628100 | HCID 178418400 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Methoxy-3-(triphenylsilyl)naphthalene | HCID 4229060 | 90% |
反応手順
A solution of 15.3 mL of sec-BuLi 1.3 M in hexane/cyclohexane (19.91 mmol) was added dropwise to a stirred solution of 3.0 g of 2-methoxynaphthalene (18.96 mmol) in 70 mL of tetrahydrofuran (THF) at a temperature of −30° C. and for a period of time of 15 min. After stirring overnight at room temperature, to the resultant tinted solution was added a solution of 5.87 g of Ph3SiCl (19.91 mmol) and 3.46 mL of hexamethylphosphoramide (HMPA) (19.88 mmol) in 50 mL of THF. The reaction mixture was heated at reflux for a period of time of 20 h, cooled and diluted with 500 mL of water. The organic part was extracted with 3 times 50 mL of Et2O. The combined organic extracts were dried over MgSO4, and evaporated. The crude residue was recrystallised from heptane and dried under vacuum to give 7.11 g of (3-methoxy-2-naphthyl)(triphenyl)silane (17.07 mmol) with a yield of 90%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08492493B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-2024b7b8d9a84ea79dc3d5622c7a1778 |
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| 出典メモ | uspto-grants-2013_07 |
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