HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl bromide → (2-Bromobenzyl) indole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | Indole-4-carboxaldehyde | HCID 333703 | — |
| Product | (2-Bromobenzyl) indole-4-carbaldehyde | HCID 54532249 | 96.6% |
Reaction Steps
The same procedures used in Example 1 were repeated except for using 3.78 g of o-bromobenzyl bromide and 2.00 g of indole-4-carbaldehyde as a starting material to give 4.18 g of (2-bromobenzyl) indole-4-carbaldehyde as pale yellow crystals. 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-5e57c3860c4940368c999dbc06a6a175 |
| Source note | uspto-grants-1998_09 |