HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-METHOXYISOBENZOFURAN-1(3H)-ONE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxyisobenzofuran-1(3H)-one | HCID 12662077 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-METHOXYISOBENZOFURAN-1(3H)-ONE | HCID 11116379 | 93.2% |
Reaction Steps
Iodomethane (1.313 mL, 20.78 mmol) was added to 4-hydroxyisobenzofuran-1(3H)-one (3.12 g, 20.78 mmol) and potassium carbonate (5.74 g, 41.56 mmol) in DMF (50 mL) at 21° C. under air. The resulting solution was stirred overnight. The solvent was removed to give a yellow solid which was then quenched with potassium carbonate (70 ml). The mixture was extracted ethyl acetate (3×75 ml). The combined extracts were evaporated to give the desired material as a yellow solid (3.18 g, 93% yield), which was used without further purification; 1H NMR (400.132 MHz, CDCl3) δ 3.30 (2H, s), 5.37 (2H, s), 7.31-7.42 (2H, m), 7.51-7.61 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129380B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-9a2fbbc23a6c42949c4723360b04603b |
| Source note | uspto-grants-2012_03 |