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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
Reactant4H-1,3-Benzodioxin-4-one, 5-hydroxy-2,2-dimethyl-HCID 11052514—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-hydroxy-6-(2,2,2-trifluoroethoxy)benzoateHCID 6931655379%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816090B2
Source datasetuspto-grants-2014_08
ORD IDord-4d1cd5aaaf314001b83c20920213a212
Source noteuspto-grants-2014_08