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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007949Generated: October 30, 2026

Hydrochloric Acid → HCID 22666364, compound

https://huagongshe.com/reaction/1007949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl chloroacetateHCID 66052—
ReactantHCID 22666446HCID 22666446—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22666364HCID 22666364—

Reaction Conditions

Temperature40 °C

Reaction Steps

In 66 mL of dimethyl sulfoxide is dissolved 15.2 g of ethyl 4-ethoxycarbonyl-2,3,6-trifluorophenylacetate, to which are added 7.84 g of potassium carbonate and 4.54 g of sodium hydrosulfide n-hydrate(purity 70%). The mixture is stirred at 40° C. for 2 hours. The reaction mixture is cooled to 5° C., 8.1 mL of tert-butyl chloroacetate is added, and the mixture thus formed is stirred at the same temperature as above for 20 minutes. Then, 6.36 g of potassium tert-butoxide is added and stirred for one hour. Water and ethyl acetate are added to the reaction mixture, pH is adjusted to 1 with 6 mol/L hydrochloric acid, 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 successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. Thus, 19.2 g of tert-butyl 6-(2-ethoxy-2-oxoethyl)-5,7-difluoro-3-oxo-2,3-dihydrobenzo[b]thiophene-2-carboxylate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-d1b3616d65464b2fa6ce0761c6c8ae85
Source noteuspto-grants-2004_09