関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Phenol | HCID 996 | — |
| 反応物 | 3,4-Dichlorobenzotrifluoride | HCID 9481 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 触媒 | Copper | HCID 23978 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-(2-Chloro-4-trifluoromethylphenoxy)benzene | HCID 12918171 | 98.5% |
反応手順
In this example 2143 g (22.77 mol) of phenol and 906 g (22.66 mol) of sodium hydroxide were mixed together in a stirred mixture of 5.5 liters of dimethyl sulfoxide and 5.5 liters of toluene at room temperature. The mixture was then heated at reflux for 54 hours. The water formed by the reaction was removed along with a substantial portion of the toluene and a small amount of the dimethyl sulfoxide (total volume collected 4910 ml of which 690 ml were water). The temperature of the remaining reaction mixture, now containing sodium phenolate, was permitted to drop to 155° C. and 44 g of powdered copper was added. 4730 g (22 mol) of 1,2-dichloro-4-trifluoromethylbenzene was then added dropwise while maintaining the reaction mixture at 153°-155° C. After addition of the 1,2-dichloro-4-trifluoromethylbenzene, the reaction mixture was maintained at 155° C. for about 30 minutes and then allowed to stand overnight (about 12 hours) at room temperature. The reaction mixture was poured onto cold 0.5% HCl. phase separated and extracted with methylene chloride. Combined organics were washed with 5% sodium hydroxide and with water, dried over magnesium sulfate and silica, and filtered. The filtrate was then stripped (evaporated) affording 5906 g of 4-(2-chloro-4-trifluoromethylphenoxy)benzene as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04289909 |
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| 出典データセット | uspto-grants-1981_09 |
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| ORD ID | ord-024198ff59e847708e99be136f3bd477 |
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| 出典メモ | uspto-grants-1981_09 |
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