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HRID 1577944作成日:2026年10月26日

Hydrochloric Acid → 4-(2-Chloro-4-trifluoromethylphenoxy)benzene

https://huagongshe.com/reaction/1577944

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物PhenolHCID 996—
反応物3,4-DichlorobenzotrifluorideHCID 9481—
反応物Sodium HydroxideHCID 14798—
触媒CopperHCID 23978—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物4-(2-Chloro-4-trifluoromethylphenoxy)benzeneHCID 1291817198.5%

反応条件

温度155 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04289909
出典データセットuspto-grants-1981_09
ORD IDord-024198ff59e847708e99be136f3bd477
出典メモuspto-grants-1981_09