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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877197Generated: October 29, 2026

Hydrochloric Acid → 4,4,4-Trifluoro-2-methyl-1-(4-methylphenyl)butan-1-one

https://huagongshe.com/reaction/877197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 15104473HCID 15104473—
Solvent1,2-DichloroethaneHCID 11—
Product4,4,4-Trifluoro-2-methyl-1-(4-methylphenyl)butan-1-oneHCID 58136598—

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., 16.44 g (123.3 mmol) of aluminum chloride were added a little at a time to 12.6 ml (118.6 mmol) of toluene and 20.9 g (119.7 mmol) of 4,4,4-trifluoro-2-methylbutanoyl chloride in 300 ml of 1,2-dichloroethane, and the mixture was stirred at 0° C. for one hour. The reaction mixture was then slowly warmed to room temperature and stirred at this temperature for three hours. The reaction mixture was then slowly added to 300 ml of ice-cooled 18.5% strength hydrochloric acid, and the organic phase was then removed. The aqueous phase was extracted three more times with dichloromethane. The combined organic phases were dried over sodium sulfate and filtered, and the solvent was removed under reduced pressure. The crude product was purified chromatographically on silica gel (mobile phase cyclohexane/ethyl acetate 4:1). This gave 19.96 g (18.7 mmol, 73% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987256B2
Source datasetuspto-grants-2015_03
ORD IDord-8691fa4028444c4fb365b9b54b027620
Source noteuspto-grants-2015_03