Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290635Generated: October 30, 2026

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

https://huagongshe.com/reaction/2290635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,4-Bis(2,2,2-trifluoroethoxy)benzeneHCID 737156—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-(2,5-Bis(2,2,2-trifluoroethoxy)phenyl)ethan-1-oneHCID 273607382%

Reaction Steps

To a mixture of 4.367 kilograms (32.75 moles) of aluminum chloride and 8.8 liters of dichloromethane at 0° C. is added gradually a solution of 3,267 kilograms of 1,4-bis(2,2,2-trifluoroethoxy)benzene and 1.899 kilograms (13.7 moles) of acetic anhydride in 1.3 liters of dichloromethane. The reaction temperature is maintained to 5° to 10° C. while stirring the mixture for about 16 hours. The reaction mixture is then heated to its reflux temperature and maintained under reflux for 4 hours. The reaction mixture is then acidified with 8.76 kilograms of 10 percent hydrochloric acid. Ice is added to the mixture to maintain the temperature below 20° C. The organic layer is separated and the aqueous layers are extracted several times with dichloromethane. The organic layers are dried, then evaporated to provide a residue which is triturated with hexane to provide a yellow solid product. Two crops of product are obtained providing a total yield of 3.088 kilograms of 2,5-bis(2,2,2 -trifluoroethoxy)acetophenone, m.p. 84° to 88° C., yield 82 percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617396
Source datasetuspto-grants-1986_10
ORD IDord-4d606833d1c145eca10755b518b8eec2
Source noteuspto-grants-1986_10