HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Methyl-5,6-dihydroindeno[2,1-b]indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5,6-Dihydroindeno[2,1-b]indole | HCID 13129410 | — |
| Catalyst | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Methyl-5,6-dihydroindeno[2,1-b]indole | HCID 13129411 | 78.2% |
Reaction Steps
In a 0.5 l bulb were placed 100 ml 50% aqueous NaOH, 100 ml benzene, 6.1 g (28 mmol)of 5,6-dihydroindeno[2,1-b]indole, prepared in Example 4, 1.8 ml (28 mmol) of MeI and 0.5 g of trimethylcetylammonium bromide. After having stirred the obtained mixture for 2 hours, the formation of an organic phase was observed; said phase was separated, washed twice with water (100 ml) and dried over Na2SO4. After removal of the solvent, the residue was recrystallized from ethanol, obtaining 4.8 g of N-methyl-5,6-dihydroindeno[2,1-b]indole (yield=78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451724B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-e5eded4ba45a4b619e3d24c9e918ebc9 |
| Source note | uspto-grants-2002_09 |