Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275666Generated: October 25, 2026

Hydrochloric Acid → HCID 178459013, compound

https://huagongshe.com/reaction/275666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4-Dimethyl-8-propoxymethyl-1,1-dioxothiochromane-7-carboxylic acidHCID 11290333—
ReactantHCID 178481816HCID 178481816—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
SolventWater ethylacetateHCID 22728543—
ProductHCID 178459013HCID 178459013—

Reaction Steps

A solution of 0.6 g (1.84 mmol) of 4,4-dimethyl-8-propoxymethyl-1,1-dioxothiochromane-7-carboxylic acid, 0.18 g (1.84 mmol) of 1-methyl-5-hydroxypyrazole and 0.38 g (1.84 mmol) of N,N-dicyclohexylcarbodiimide in 20 ml of acetonitrile was stirred at room temperature for 12 hours. The reaction mixture was subsequently stirred into a mixture of ethyl acetate and 2% strength aqueous sodium carbonate solution, and the precipitate which formed was filtered off with suction. The organic phase of the filtrate was dried and the solvent was distilled off. The resulting residue was dissolved in 5 ml of 1,4-dioxane, 0.51 g (3.7 mmol) of potassium carbonate were added and the mixture was heated under reflux for 4 hours. After cooling, the reaction mixture was taken up in ethyl acetate/water, and the aqueous phase was adjusted to pH 3 using 2N hydrochloric acid and subsequently extracted with ethyl acetate. The extract was dried and the solvent was removed, giving a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352959B1
Source datasetuspto-grants-2002_03
ORD IDord-ca51a17ce07a432b9c1203447caffd70
Source noteuspto-grants-2002_03