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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249071Generated: October 30, 2026

Hydrochloric Acid → 4-Hydroxy-6-(4-trifluoromethylphenylthio)2-hexanone

https://huagongshe.com/reaction/2249071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant3-(4-Trifluoromethylphenylthio)propanalHCID 14347982—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-Hydroxy-6-(4-trifluoromethylphenylthio)2-hexanoneHCID 1453447280.9%

Reaction Steps

3.77 Grams of methyl acetoacetate were dissolved in 5 ml of water, and 4.5 g of a 30% aqueous sodium hydroxide solution were added thereto by drops while cooling the mixture to 35° C. or less. After having been stirred at 30°-35° C. for 3 hours, the mixture was adjusted to pH 7.5 with a concentrated aqueous hydrochloric acid solution. Thereafter, 0.31 g of sodium acetate and 0.54 g of benzyltriethylammonium chloride were added thereto and then 14.7 g of a toluene solution containing 39.8% of 3-(4-trifluoromethylphenylthio)propanal were added thereto. The mixture was stirred at 45°-50° C. for 6 hours and then at room temperature for 12 hours. After the mixture had been neutralized with a concentrated aqueous hydrochloric acid solution, the organic layer was separated, washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. Removing the solvent from the layer under reduced pressure gave crude 4-hydroxy-6-(4-trifluoromethylphenylthio)-2-hexanone in a yield of 80.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041679
Source datasetuspto-grants-1991_08
ORD IDord-e4b7fb5eaa644dca80c7e464ebadaf9d
Source noteuspto-grants-1991_08