化工社化工社 化学情報印刷レポート · 研究参考用
Methyl iodide → 1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Trimethyl orthoformate | HCID 9005 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3'-Bromo-4'-hydroxy-5'-(trifluoromethyl)acetophenone | HCID 58085700 | — |
| 触媒 | D-Camphorsulfonic Acid | HCID 65617 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Heptane water | HCID 57468513 | — |
| 生成物 | 1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzene | HCID 58085697 | — |
反応手順
1-(3-Bromo-4-hydroxy-5-trifluoromethylphenyl)ethanone (O4.004; 6.8 g) was dissolved in methanol (50 ml) and admixed successively with DL-10-camphorsulfonic acid (111 mg) and trimethyl orthoformate (8 ml). After stirring at RT for 2 h, DMF (75 ml), potassium carbonate (4.98 g) and then slowly, while cooling with ice, iodomethane (3 ml) were added. After stirring at RT for 4 h, the reaction mixture was left to stand overnight and then admixed with n-heptane/water, and the organic phase was removed. The aqueous phase was extracted by shaking once more with n-heptane, and the combined organic phases were then dried over magnesium sulfate, filtered and concentrated. 7 g of the title compound were obtained in sufficient purity.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08076336B2 |
| 出典データセット | uspto-grants-2011_12 |
| ORD ID | ord-5992c9e592904eba8876e241466c6e2e |
| 出典メモ | uspto-grants-2011_12 |