HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(4-Hydroxyphenylthio)-7-isopropoxy-5-methoxychromone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Reactant | 7-Isopropoxy-5-methoxy-2-methylsulfinylchromone | HCID 22906467 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(4-Hydroxyphenylthio)-7-isopropoxy-5-methoxychromone | HCID 22906489 | 57.7% |
Reaction Steps
A mixture of 146 mg of 7-isopropoxy-5-methoxy-2-methylsulfinylchromone (0.493 mmol ) , 93 mg of 4-hydroxybenzenethiol(0.740 mmol), 102 mg of potassium carbonate (0.740 mmol) and 6 ml acetone was stirred for 2 hours at room temperature. The reaction solution was neutralized with dilute hydrochloric acid and extracted twice with ethyl acetate, and the organic layer was washed with saturated NaCl water and was then dried over sodium sulfate anhydride. The solvent was distilled off under reduced pressure, and the crude product was subjected to recrystallization from acetone-methanol, to give 102 mg of 2-(4-hydroxyphenylthio)-7-isopropoxy-5-methoxychromone (57% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521216 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-b75679b73f6449178d2300d616707cb5 |
| Source note | uspto-grants-1996_05 |