HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole-3-Carboxaldehyde → HCID 18973550, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | HCID 18973462 | HCID 18973462 | — |
| Product | HCID 18973550 | HCID 18973550 | — |
Reaction Steps
The same procedures used in Example 1 were repeated except for using 435 mg of indole-3-carbaldehyde and 4-benzyloxybenzyl methanesulfonate in place of the benzyl bromide used in Example 1 to give 626 mg of 1-(4-benzyloxybenzyl)indole-3-carbaldehyde as colorless crystals. The yield thereof was found to be 61%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811439 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-603dc0aba62a4232b32214a9cba821cf |
| Source note | uspto-grants-1998_09 |