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HRID 236074생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/236074

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetic AnhydrideHCID 7918—
반응물1,4-Bis(2,2,2-trifluoroethoxy)benzeneHCID 737156—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물1-(2,5-Bis(2,2,2-trifluoroethoxy)phenyl)ethan-1-oneHCID 273607390%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04642384
출처 데이터셋uspto-grants-1987_02
ORD IDord-f7ec070462b641cbb6d46d534985f8bc
출처 메모uspto-grants-1987_02