HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249062Generated: October 28, 2026
Acetoacetic Acid → 4-Hydroxy-6-(4-trifluoromethylphenylthio)2-hexanone
https://huagongshe.com/reaction/2249062
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetoacetic Acid | HCID 96 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-(4-Trifluoromethylphenylthio)propanal | HCID 14347982 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Hydroxy-6-(4-trifluoromethylphenylthio)2-hexanone | HCID 14534472 | 85.6% |
Reaction Steps
1.51 Grams of acetoacetic acid were dissolved in 2 ml of water, and 1.82 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 6 hours, the mixture was adjusted to pH 7.5 with a concentrated aqueous hydrochloric acid solution. Thereafter, 0.08 g of sodium acetate and 0.32 g of tetrabutylammonium bromide were added thereto and then 5.82 g of a toluene solution containing 40.2% 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 3.02 g of crude 4-hydroxy-6-(4-trifluoromethylphenylthio)-2-hexanone (purity: 82.8%, yield: 85.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05041679 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-712e86ab69da4c36b241ab1dd26dcf82 |
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| Source note | uspto-grants-1991_08 |
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