HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Isopropoxy-5-methoxy-2-methylthiochromone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5,7-Dihydroxy-2-methylthiochromone | HCID 136102411 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Isopropoxy-5-methoxy-2-methylthiochromone | HCID 57010221 | 54.6% |
Reaction Steps
354 mg of 5,7-dihydroxy-2-methylthiochromone (1.58 mmol), 1.09 g of potassium carbonate (7.90 mmol), 0.79 ml isopropyl iodide (7.90 mmol) and 20 ml acetone were refluxed overnight. After addition of 2.95 ml methyl iodide (47.4 mmol), the mixture was further refluxed overnight. Following addition of water, the reaction solution was extracted twice with ethyl acetate, and 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 purified by flash column chromatography (hexane: ethyl acetate =1 : 3→1:6), to give 228 mg of 7-isopropoxy-5-methoxy-2-methylthiochromone (52% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521216 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-cd9e66d801a844cdb53d2a0b23236fdc |
| Source note | uspto-grants-1996_05 |