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Sodium Hydroxide → 3-Phenoxy-4-fluorobenzyl 2-(4-trifluoromethoxyphenyl)-2-methylpropyl ether
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 4-(Bromomethyl)-1-fluoro-2-phenoxybenzene | HCID 12922714 | — |
| 反応物 | 2-Methyl-2-(4-(trifluoromethoxy)phenyl)propan-1-ol | HCID 14155774 | — |
| 触媒 | Benzyltriethylammonium bromide | HCID 165294 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-Phenoxy-4-fluorobenzyl 2-(4-trifluoromethoxyphenyl)-2-methylpropyl ether | HCID 14155770 | 77% |
反応手順
1.4 g of 2-(4-trifluoromethoxyphenyl)-2-methylpropyl alcohol prepared in the above step (1), 2.6 g of 3-phenoxy-4-fluorobenzyl bromide and 0.6 g of triethylbenzylammonium bromide were added to 20 ml of a 50% aqueous NaOH solution and the mixture was stirred at room temperature for 3 h. Water was added thereto. After extracting with benzene, the benzene solution was washed with a dilute hydrochloric acid solution and then water and dried. Benzene was distilled off under reduced pressure and 3.6 g of an oily product thus obtained was purified according to column chromatography [silica gel, developer: toluene/hexane (1:4)] to obtain 2.0 g of 3-phenoxy-4-fluorobenzyl 2-(4-trifluoromethoxyphenyl)-2-methylpropyl ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04997650 |
| 出典データセット | uspto-grants-1991_03 |
| ORD ID | ord-8b40d9310901416d8c6b7e01724df191 |
| 出典メモ | uspto-grants-1991_03 |