HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1H-Indole, 1-methyl-5-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Nitroindole | HCID 22523 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1H-Indole, 1-methyl-5-nitro- | HCID 147322 | 92.3% |
Reaction Steps
To a solution of 5-nitro-1H-indole (2.0 g, 12.3 mmol) in acetone (20 ml), powdered potassium hydroxide (3.4 g, 60.7 mmol, 5 eq) was added followed by the addition methyl iodide (2.61 g, 18.5 mmol, 1.5 eq) at 0° C. The reaction mixture was heated to reflux for 10 hr. The solvent was evaporated and water was added. The compound was extracted with ethyl acetate, dried over anhydrous sodium sulphate, filtered and the organic layer was concentrated to dryness to yield 1-methyl-5-nitro-1H-indole (2.0 g, 92%). The crude compound was used in the next stage without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486962B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-d8e3e3273a2a424b9bffb4005c02104d |
| Source note | uspto-grants-2013_07 |