HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 1-Ethyl-1H-indole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Ethyl-1H-indole-3-carbaldehyde | HCID 599090 | 80% |
Reaction Steps
1-ethylindole-3-carboxaldehyde was prepared from alkylation reaction of indole-3-carboxaldehyde. Indole-3-carboxaldehyde (900 mg, 6.2 mmol) was dissolved in 5 ml dimethylformamide, ethyl bromide (918 μl, 12 mmol) and sodium hydride (282.8 mg, 12 mmol) were added to the reaction mixture. Solution was stirred and refluxed for three hours. The reaction mixture was then evaporated to dryness and washed with water. Pale brown crystals were obtained with 80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06767909B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-40882a553ceb4b4b93ed98acb4a6c827 |
| Source note | uspto-grants-2004_07 |