HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5,7-Dihydroxy-2-(4-hydroxyphenylthio)chromone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Reactant | 5,7-Dihydroxy-2-methylsulfinylchromone | HCID 22906488 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5,7-Dihydroxy-2-(4-hydroxyphenylthio)chromone | HCID 22906462 | 36% |
Reaction Steps
A mixture of 32 mg of 5,7-dihydroxy-2-methylsulfinylchromone (0.134 mmol), 20 mg of 4-hydroxybenzenethiol (0.161 mmol), 41 mg of potassium carbonate (0. 295 mmol) and 2 ml acetone was stirred overnight at room temperature. The reaction solution was neutralized with dilute hydrochloric acid and then extracted twice with ethyl acetate. The organic layer was washed with saturated NaCl water and dried over sodium sulfate anhydride. The solvent was distilled off under reduced pressure, and the crude product was subjected to recrystallization from acetone-hexane, to give 14.6 mg of 5,7-dihydroxy-2-(4-hydroxyphenylthio)chromone (36% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521216 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-0d726f084be9443a8d4285eff3c513d6 |
| Source note | uspto-grants-1996_05 |