HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamide | HCID 9824373 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-benzamide | HCID 9868421 | 87% |
Reaction Steps
To a solution of 100 mg (0.23 mmol) 2-benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamide in 1 ml N,N-dimethylformamide at 0° C. were added 50 mg (0.25 mmol) potassium hexamethyldisilazide. Stirring was continued for 1 h at this temperature and 0.016 ml (0.25 mmol) methyl iodide were added. After stirring for 3 h at room temperature, ethyl acetate was added. The mixture was washed with brine, dried (magnesium sulfate) and evaporated. The solvent was removed in vacuo and the residue was purified by flash chromatography to give 90 mg (87%) of the title compound as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06407111B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-06075aa6fa864525aa5621d3f988052f |
| Source note | uspto-grants-2002_06 |