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HRID 236074作成日:2026年10月27日

Hydrochloric Acid → 1-(2,5-Bis(2,2,2-trifluoroethoxy)phenyl)ethan-1-one

https://huagongshe.com/reaction/236074

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Acetic AnhydrideHCID 7918—
反応物1,4-Bis(2,2,2-trifluoroethoxy)benzeneHCID 737156—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
生成物1-(2,5-Bis(2,2,2-trifluoroethoxy)phenyl)ethan-1-oneHCID 273607390%

反応手順

To a mixture of 2.43 moles (324 g.) of aluminum chloride in 648 ml. of dichloromethane is added a solution of 0.88 mole (274 g.) of 1,4-bis(2,2,2-trifluoroethoxy)benzene and 0.97 mole (92 ml.) of acetic anhydride in 880 ml. of dichloromethane over a 3 hour period while maintaining the temperature at above 0° C. The reaction mixture is then heated to its reflux temperature and stirred at reflux for 5 hours. The progress of the reaction is followed using thin-layer chromatography. The reaction mixture is placed in an ice bath and ice and 10 percent hydrochloric acid are added slowly to decompose the aluminum chloride complex. The temperature of the reaction mixture is not allowed to exceed 25° C. The organic phase is separated and washed once with 2 liters of 10 percent hydrochloric acid and then with 2 liters of water. The combined aqueous phase is extracted with several liters of dichloromethane. The organic phase is dried over magnesium sulfate, then evaporated to provide a moist residue. Hexane is added to the residue and the resulting solid is collected by filtration and washed with hexane. Upon drying, 250 g. of light yellow crystalline 2,5-bis(2,2,2-trifluoroethoxy)acetophenone is obtained. The yield is 90 percent, the m.p. is 84° to 86° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04642384
出典データセットuspto-grants-1987_02
ORD IDord-f7ec070462b641cbb6d46d534985f8bc
出典メモuspto-grants-1987_02