HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410317Generated: November 1, 2026
Hydrochloric Acid → Methyl 2-hydroxy-6-(2,2,2-trifluoroethoxy)benzoate
https://huagongshe.com/reaction/2410317
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
| Reactant | 4H-1,3-Benzodioxin-4-one, 5-hydroxy-2,2-dimethyl- | HCID 11052514 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-hydroxy-6-(2,2,2-trifluoroethoxy)benzoate | HCID 69316553 | 79% |
Reaction Steps
A mixture of 5-hydroxy-2,2-dimethyl-4H-1,3-benzodioxin-4-one (123 g, 633 mmol, Synth. Commun. 1994, 24, 1025), potassium carbonate (262 g, 1.9 mol) and 2,2,2-trifluoroethyl trifluoromethanesulfonate (95.8 mL, 665 mmol) in N,N-dimethylformamide (600 mL) was stirred at 50° C. for 30 min. Then methanol (300 mL) was added to the mixture, and stirring was continued for 5 h at that temperature. After cooling to room temperature, the mixture was diluted with water (500 mL) and neutralized with 2N hydrochloric acid. Product was extracted with a mixture of ethyl acetate-hexane (5:1, 500 mL×3). Combined organic layers were washed with water (500 mL), dried over magnesium sulfate and concentrated under reduced pressure. The residual solid was recrystallized from methanol-water to afford 125 g (79%) of the desired product as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816090B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-4d1cd5aaaf314001b83c20920213a212 |
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| Source note | uspto-grants-2014_08 |
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