HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 18973345, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Methyl indole-6-carboxylate | HCID 639844 | — |
| Product | HCID 18973345 | HCID 18973345 | 19.1% |
Reaction Steps
The same procedures used in Example 1 were repeated except for using 2.00 g of methyl indole-6-carboxylate and 2.54 g of phenethyl bromide instead of the indole-4-carbaldehyde and benzyl bromide used in Example 1 to give 0.61 g of methyl 1-phenethylindole-6-carboxylate as a yellow oily substance. The yield thereof was found to be 19%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811439 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-c15ad290fcac4a1ba70c1e96cc0fcc3a |
| Source note | uspto-grants-1998_09 |