HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 14914492, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Product | HCID 14914492 | HCID 14914492 | 105.5% |
Reaction Steps
The same procedures used in Example 7 were repeated except for using 2.00 g of indole-3-carbaldehyde instead of the indole-4-carbaldehyde used in Example 7 and 2.35 g of 2-phenethyl bromide to give 3.34 g of 1-phenethylindole-3-carbaldehyde as a brown oily substance. The yield thereof was found to be 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811439 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-5a8fab8a5f4a4915a765bba95404bcad |
| Source note | uspto-grants-1998_09 |