化工社化工社 化学情報印刷レポート · 研究参考用
Acetone → 2,6-Diallyl4-benzyloxyphenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | Monobenzone | HCID 7638 | — |
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 生成物 | 2,6-Diallyl4-benzyloxyphenol | HCID 21985951 | — |
反応手順
To a solution of starting 4-benzyloxyphenol (20 g) in acetone (800 mL) were added allylbromide (50 mL) and K2CO3 (60 g). The reaction mixture was refluxed overnight. After cooling to the room temperature, the insoluble materials were removed by filtration. The filtrate was concentrated in vac. The residue was partitioned between ethyl ether (500 mL) and 2N aqueous NaOH (200 mL). The organic layer was washed with water and brine, dried over anhydrous MgSO4, filtered, and concentrated in vac. to give the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091230B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-1782f4c6e18d44388356e24fbc39135b |
| 出典メモ | uspto-grants-2006_08 |