HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19980329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl (2-methyl-6-nitroanilino)(oxo)acetate | HCID 15525662 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19980329 | HCID 19980329 | — |
Reaction Steps
NaH (1 g, 22 mmol) was added in portions to a stirred solution of N-ethoxalyl-2-nitro-6-methylaniline (5 g, 20 mmol) in DMF (50 ml). Methyl iodide (2 ml, 22 mmol) was thereafter added. The mixture was left overnight at room temperature, whereafter the solvent was removed by evaporation in vacuo. The residue was partitioned between ether and water. The organic phase was washed with water, dried over Na2SO4 and evaporated to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075304 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-96a5e5041e784b8e8bfb7cb94618e03d |
| Source note | uspto-grants-1991_12 |