HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2,2,2-trifluoro-N-(4-iodophenyl)-N-methylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2,2-trifluoro-N-(4-iodophenyl)acetamide | HCID 686962 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,2,2-trifluoro-N-(4-iodophenyl)-N-methylacetamide | HCID 21071238 | — |
Reaction Steps
Part B: The above-obtained amide was dissolved in acetone (80 mL), to which potassium carbonate (15.75 g, 114.1 mmol) and iodomethane (9.6 mL, 114.1 mmol) were added. The reaction was heated to reflux for 2 hours and cooled, and the resulting solid was filtered. The solvent was removed from the filtrate. The residue was dissolved in dichloromethane, washed with water and brine, and dried over sodium sulfate. After filtration and removal of solvent, the solid was further dried in vacuo to give the desired 2,2,2-trifluoro-N-(4-iodo-phenyl)-N-methyl-acetamide as a white solid. MS found: (M+1)+=330.05.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157470B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-cb5d0e061ce44144a6d498328cbc0a74 |
| Source note | uspto-grants-2007_01 |