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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721115Generated: October 31, 2026

Hydrochloric Acid → 4,4-Difluoro-1-(4-trifluoromethylphenyl)butane-1,3-dione

https://huagongshe.com/reaction/1721115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl difluoroacetateHCID 9961—
Reactant1-(4-(Trifluoromethyl)phenyl)ethan-1-oneHCID 69731—
ReactantSodium MethoxideHCID 10942334—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4,4-Difluoro-1-(4-trifluoromethylphenyl)butane-1,3-dioneHCID 1892036991%

Reaction Steps

Ethyl difluoroacetate (2.78 g, 22.4 mmol) was placed in a 100 mL round bottom flask and dissolved in ether (10 mL). To the stirred solution was added 25 weight % sodium methoxide (6.02 g, 27.8 mmol) followed by 4'-(trifluoromethyl)acetophenone (3.80 20.2 mmol) and THF (20 mL). The reaction was stirred at room temperature overnight (15.6 hours), then treated with 3N HCl (20 mL). The organic layer was collected and washed with brine, dried over HgSO4, concentrated in vacuo to give a brown oil (4.88 g, 91%). 1H NMR (acetone d6) 300 MHz 15.10 (br s, 1H), 8.03 (d, J=8.7 Hz, 2H), 7.77 (d, J=8.5 Hz, 2H), 6.59 (s, 1H), 6.02 (t, J=54.2 Hz, 1H); 19F NMR (acetone d6) 300 MHz: -63.70 (s), -127.10 (d); M+266.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508426
Source datasetuspto-grants-1996_04
ORD IDord-b774cd0279a24a97a1a9b84fb40f64f6
Source noteuspto-grants-1996_04