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Toluene → 6-(3,4-Difluorophenyl)-2-naphthol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| 反応物 | 3,4-Difluorophenylboric acid | HCID 21869672 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-(3,4-Difluorophenyl)-2-naphthol | HCID 21870820 | 88.1% |
反応手順
To 25.0 g of 6-bromo-2-naphthol and 22.0 g of 3,4-difluorophenylboric acid were added 100 ml of toluene, 50 ml of ethanol, 50 ml of a 2 N aqueous solution of potassium carbonate and 1.3 g of tetrakis(triphenylphosphine)palladium (0). The reaction mixture was heated under reflux for 3 hours. The reaction solution was then allowed to cool to room temperature. The resulting organic phase was separated, washed with water and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was then distilled off. The residue was purified through silica gel column chromatography (dichloromethane) to obtain 25.3 g of 6-(3,4-difluorophenyl)-2-naphthol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06468607B1 |
| 出典データセット | uspto-grants-2002_10 |
| ORD ID | ord-49778d7a77264410acd17cf44f6a8f6c |
| 出典メモ | uspto-grants-2002_10 |