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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079022Generated: October 31, 2026

p-Toluenesulfonic acid → Ethyl 6,6,6-trifluoro-3-oxohexanoate

https://huagongshe.com/reaction/1079022

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
Reactant4,4,4-Trifluorobutyrylmalonic acidHCID 18970911—
SolventWaterHCID 962—
ProductEthyl 6,6,6-trifluoro-3-oxohexanoateHCID 1897091324,903.6%

Reaction Steps

A mixture of 179 g of the 4,4,4-trifluorobutyrylmalonic acid ditheyl ester thus obtained, 260 ml of water and 322 mg of p-toluenesulfonic acid was refluxed with vigorous stirring for 6 hours. The reaction solution was then poured into saturated aqueous sodium hydrogencarbonate solution and extracted three times with diethyl ether. The ether layers were combined and the combined layer was washed with brine, dried over anhydrous magnesium sulfate. After the drying agent was removed, the solvent was removed under reduced pressure. The obtained residue was distilled inder reduced pressure to yield 98.8 g of the desired ethyl 4,4,4-trifluorobutyrylacetate in a yield of 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550258
Source datasetuspto-grants-1996_08
ORD IDord-14b67357ee6d4d22a27ae8c54587bce1
Source noteuspto-grants-1996_08