HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-Acetyl-4-methoxyacetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-Acetyl-4-hydroxyphenyl)acetamide | HCID 81720 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Acetyl-4-methoxyacetanilide | HCID 2817418 | 100% |
Reaction Steps
Methyl iodide (3.42 ml, 7.81 g, 55 mmol) was added to a stirred mixture of N-(3-acetyl-4-hydroxyphenyl)acetamide (J.Org.Chem. 1995, 60, 4324-4330) (9.65 g, 50 mmol) and potassium carbonate (13.82 g, 100 mmol) in dimethylformamide (50 ml). The mixture was stirred at room temperature for 72 hours, then the solvent was evaporated under reduced pressure. Water (100 ml) was added and the mixture was extracted with ethyl acetate (6×100 ml). The combined organic fractions were dried (MgSO4) and evaporated under reduced pressure to give N-(3-acetyl-4-methoxyphenyl)acetamide as a tan solid (10.34 g, 100%), 1H NMR (d6 -DMSO) δ 9.91 (1H, br. s), 7.76 (2H, m), 7.12 (1H, d, J=9.6 Hz), 3.86 (3H, s), 2.52 (3H, s), and 2.01 (3H, s). m/e (CI+) 208 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06096766 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-968a67cf23a345b4b7bec1c6c7034b40 |
| Source note | uspto-grants-2000_08 |