HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 3-Ethyl-1,1,2-trimethyl-1H-benzo(e)indol-3-ium Iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 2,3,3-Trimethylbenzoindolenine | HCID 170530 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Ethyl-1,1,2-trimethyl-1H-benzo(e)indol-3-ium Iodide | HCID 10090215 | 91.3% |
Reaction Steps
Ethyl iodide (1.1 g, 7.2 mmol) was added to an acetonitrile solution (40 ml) of 1,1,2-trimethylbenz[e]indole (1) (1.0 g, 4.8 mmol, Daiichi Pure Chemicals Co., Ltd.), and then the mixture was heated under reflux for 2 days. The reaction mixture was concentrated under reduced pressure, and ether (80 ml) was added to the residue. The resulting solid was repeatedly washed with ether to obtain the title compound (2) as a dark violet solid (1.6 g, 91%). mp. 213-218° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403625B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-9d9cbc1d84c94af69f860275d98eabac |
| Source note | uspto-grants-2002_06 |