化工社化工社 化学情報印刷レポート · 研究参考用
P-Toluic Acid → (4-Methoxyphenyl)(4-methylphenyl)methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | P-Toluic Acid | HCID 7470 | — |
| 反応物 | Anisole | HCID 7519 | — |
| 反応物 | Trifluoromethanesulfonic acid | HCID 62406 | — |
| 反応物 | Praseodymium(III) trifluoromethanesulfonate | HCID 9894708 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (4-Methoxyphenyl)(4-methylphenyl)methanone | HCID 32113 | 60% |
反応手順
Praseodymium (III) trifluoromethanesulfonate (1.18 g as a wet solid), trifluoromethanesulfonic acid (0.30 g), anisole (2.38 g) and para-toluic acid (2.72 g) were refluxed together in 175 mL toluene with azeotropic removal of the lower water layer (Dean-Stark apparatus). After 22 hours, the mixture was cooled and extracted with 3×25 mL water, then by 2×25 mL saturated sodium bicarbonate solution. The organic layer was dried using anhydrous sodium sulfate, filtered, then concentrated down in vacuo to give crude 4-methoxy-4′-methylbenzophenone (2.7 g, 60% yield) as a cream-colored crystalline solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06362375B1 |
| 出典データセット | uspto-grants-2002_03 |
| ORD ID | ord-e10a51f8067e4e7f92269219d2b85cb0 |
| 出典メモ | uspto-grants-2002_03 |