HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 69817507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 3H-Indole, 2,3,3-trimethyl-5-nitro- | HCID 97551 | — |
| Product | HCID 69817507 | HCID 69817507 | 53.1% |
Reaction Steps
5-Nitro-2,3,3-trimethylindole (518 mg, 2.54 mmol) and ethyl iodide (2.5 ml, 4.85 g, 31 mmol, excess) were mixed and heated to reflux for 8 hours. After cooling to room temperature the excess ethyl iodide was removed by a gentle nitrogen stream and the residue was dissolved in chloroform and filtered through a plug of silica. The silica was washed with chloroform (1 volume) and the combined filtrates were rotary evaporated to give the product as a yellow oil, (486 mg, 1.35 mmol, 53% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06828116B1 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-b6ee575cc8b64a39b932c7da96354243 |
| Source note | uspto-grants-2004_12 |