HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275666Generated: October 25, 2026
Hydrochloric Acid → HCID 178459013, compound
https://huagongshe.com/reaction/275666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,4-Dimethyl-8-propoxymethyl-1,1-dioxothiochromane-7-carboxylic acid | HCID 11290333 | — |
| Reactant | HCID 178481816 | HCID 178481816 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | HCID 178459013 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352959B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-ca51a17ce07a432b9c1203447caffd70 |
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| Source note | uspto-grants-2002_03 |
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