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HRID 1381043作成日:2026年10月26日

1-Chloro-4-(trifluoromethyl)benzene → 2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate

https://huagongshe.com/reaction/1381043

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
反応物Potassium CarbonateHCID 11430—
反応物2-(2-Fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionateHCID 13278922—
溶媒DimethylformamideHCID 6228—
生成物2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionateHCID 13132188—

反応条件

温度95 °C

反応手順

33.4 g of 2-(2-fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionate were dissolved in 120 ml of dimethylformamide, 15.2 g of potassium carbonate were added thereto, then the mixture was heated at 95° C. for one hour with stirring. 27.1 g of 4-trifluoromethyl chlorobenzene were added to the solution which was then heated to 95° to 100° C. for five hours. After cooling the reaction solution to room temperature, it was poured into ice-water, then extracted with toluene. The toluene layer was washed successively with 1% strength by weight sodium hydroxide solution and water, and was dried and filtered. The toluene was distilled off under reduced pressure, and further volatile by-products were removed at 100° C./0.1 mmHg. The end product of 2-(2-fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate was obtained in a yield of 20.7 g. (nD20 1.5235)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04584396
出典データセットuspto-grants-1986_04
ORD IDord-f798672ae9b74ad3ba97d7e3b13fbc29
出典メモuspto-grants-1986_04