HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(phenylmethoxy)-1H-indole-3-carbaldehyde → 4-Methylbenzyloxylindole-3-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(phenylmethoxy)-1H-indole-3-carbaldehyde | HCID 81398 | — |
| Reactant | N-methyl-N-phenethyl-2-(5-indolyloxy)acetamide | HCID 19372247 | — |
| Reactant | 5-((4-Methylbenzyl)oxy)-1H-indole-3-carbaldehyde | HCID 19372258 | — |
| Reactant | 5-(4-Methylbenzyloxy)indole | HCID 19372380 | — |
| Product | 4-Methylbenzyloxylindole-3-carboxaldehyde | HCID 86749115 | — |
Reaction Steps
When N-methyl-N-phenethyl-2-(5-indolyloxy)acetamide is replaced in the procedure of Example 6 with 5-benzyl-oxyindole and 5-(4-methylbenzyloxy)indole then the products obtained are 5-benzyloxyindole-3-carboxaldehyde and 5-(4-methylbenzyloxy)indole-3-carboxaldehyde. NMR confirms these structures.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468898 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-eed06a9c2f9c4578a77cd8b85477ad26 |
| Source note | uspto-grants-1995_11 |