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2-(Benzyloxy)-6-bromonaphthalene → 2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-diene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(Benzyloxy)-6-bromonaphthalene | HCID 640595 | — |
| 反応物 | 4-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyloxy)-tosylate | HCID 86759366 | — |
| 触媒 | copper(I) bromide | HCID 24593 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-diene | HCID 20632154 | — |
反応手順
To a solution of 4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyl)-tosylate (10), (1 equi) and copper (I) bromide (0.05 equi.) in THF (2 mL/mmole), a solution of buta-1,3-diene-2-magnesium chloride, prepared as described in (3), (38) (0.5M in THF) (1.3 equi.) was added at ice temperature over a period of 20 min. The reaction mixture was stirred at room temperature for 24 h, quenched with 5% aqueous ammonium chloride (1 mL/mmole), extracted with hexane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (hexane) gave 2-(5,5,6,6,7,7,8,8,8-nona fluoro-octyl)-buta-1,3-diene (39) a colorless oil (96%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06703082B1 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-b0fae634104f4e8badaca1a75ce245db |
| 出典メモ | uspto-grants-2004_03 |