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2-Hydroxy-4-methoxybenzophenone → {4-Methoxy-2-[(prop-2-en-1-yl)oxy]phenyl}(phenyl)methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Hydroxy-4-methoxybenzophenone | HCID 4632 | — |
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Allyl chloride | HCID 7850 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | {4-Methoxy-2-[(prop-2-en-1-yl)oxy]phenyl}(phenyl)methanone | HCID 14227056 | — |
反応手順
2-Hydroxy-4-methoxybenzophenone (114 parts) was dissolved in tetrahydrofuran (100 parts). Potassium hydroxide (30.9 parts) was added. By heating and stirring, complete dissolution was achieved. Allyl chloride (46.4 parts) and potassium iodide (4.2 parts) were added to this solution, which was then heated and refluxed for 8 hours. After cooling, it was washed with water and the solvent was removed by distillation. A crude product of the desired 2-allyloxy-4-methoxybenzophenone was obtained. It was recrystallized in n-hexane to obtain 125 parts of 2-allyloxy-4-methoxybenzophenone (melting point 40° C.) at 93% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04467082 |
| 出典データセット | uspto-grants-1984_08 |
| ORD ID | ord-b194dbbb179640d88942b8ef085f31a9 |
| 出典メモ | uspto-grants-1984_08 |