HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-fluoro-7-iodo-6-methoxybenzofuran-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-fluoro-6-hydroxy-7-iodobenzofuran-3(2H)-one | HCID 71278587 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-fluoro-7-iodo-6-methoxybenzofuran-3(2H)-one | HCID 71278801 | 23.7% |
Reaction Steps
A solution of 5-fluoro-6-hydroxy-7-iodobenzofuran-3(2H)-one (0.256 g, 0.871 mmol) in DMF (5 mL) was added with potassium carbonate (0.110 g, 0.796 mmol). The mixture was added with dimethyl sulfate (0.0803 g, 0.637 mmol) at room temperature, and the mixture was stirred for 12 hours. The reaction mixture was added with water, the mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, then the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain 5-fluoro-7-iodo-6-methoxybenzofuran-3(2H)-one (0.0582 g, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156827B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-54f1f25a2bb7421493215ab53b3700f8 |
| Source note | uspto-grants-2015_10 |