HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-Methyl-2-nitro-4-(trifluoromethoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Nitro-4-(trifluoromethoxy)aniline | HCID 2775772 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Methyl-2-nitro-4-(trifluoromethoxy)aniline | HCID 53216875 | 76.3% |
Reaction Steps
To a mixture of 2.22 g of 2-nitro-4-trifluoromethoxyaniline and 20 ml of DMF was added 0.44 g of sodium hydride (60% oily), and the mixture was stirred for 10 minutes under ice cool. To this mixture was added 1.42 g of methyl iodide, then, the mixture was stirred for 1 hour at room temperature. Into the reaction mixture, a saturated ammonium chloride aqueous solution was poured, and the mixture was extracted three times with ethyl acetate. The organic layer was dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.80 g of N-methyl-2-nitro-4-trifluoromethoxyaniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461181B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-2c8ad0f26c45424e934a1ca4998020e2 |
| Source note | uspto-grants-2013_06 |