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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007948Generated: October 29, 2026

Hydrochloric Acid → HCID 22666446, compound

https://huagongshe.com/reaction/1007948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl ethyl malonateHCID 96345—
Reactant2,3,4,5-Tetrafluorobenzoic acidHCID 297549—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22666446HCID 22666446—

Reaction Conditions

Temperature70 °C

Reaction Steps

In 50 mL of dimethyl sulfoxide is dissolved 2,3,4,5-tetrafluorobenzoic acid, to which are added 4.6 mL of bromoethane and 8.19 g of potassium carbonate. The mixture is stirred at 70° C. for 2 hours. Then, 18.52 g of potassium carbonate and 15.02 g of tert-butyl ethyl malonate, and the mixture is stirred at 90° C. for 2 hours. Water and toluene are added to the reaction mixture, pH is adjusted to 4 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer is washed with water, saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, the solvent is distilled off under reduced pressure, and the residue is dissolved in 50 mL of toluene and heated under reflux for 3.5 hours together with 0.2 g of p-toluenesulfonic acid monohydrate. Water and ethyl acetate are added to the reaction mixture, and the organic layer is separated. The organic layer is washed with water, saturated aqueous solution of sodium bicarbonate and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. By distilling off the solvent under reduced pressure, there is obtained 15.2 g of ethyl 4-ethoxycarbonyl-2,3,6-trifluorophenylacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-9123813231e24943b7234e0acf2c047b
Source noteuspto-grants-2004_09