HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-Methyl-6-nitro-1H-indol-3-yl)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1h-Indole-3-acetonitrile, 6-nitro- | HCID 252385 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1-Methyl-6-nitro-1H-indol-3-yl)-acetonitrile | HCID 21999030 | 98.8% |
Reaction Steps
65.5 g (0.474 mol) of powdered potassium carbonate was added to a solution of 28.9 g (0.143 mol) of (6-nitro-1H-indol-3,yl)-acetonitrile (13) from Step C above in 230 ml of dimethylformamide at room temperature. The suspension was stirred for 40 minutes then 25.48 g (0.179 mol) of methyl iodide was added dropwise over 65 minutes. After stirring at room temperature over night the reaction mixture was cooled and poured into a total of 600 ml of water. The precipitate was filtered, washed with a little water and dried on phosphor anhydride until reaching constant weight. The procedure yielded 30.4 g (95.4%) of (1-methyl-6-nitro-1H-indol-3-yl)acetonitrile (14), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048887 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-9b1f4588515e487bb45d15caee771637 |
| Source note | uspto-grants-2000_04 |