HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-methyl-2-pentene → 1-(4-Methyl-3-pentenyl)indole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-methyl-2-pentene | HCID 137521 | — |
| Reactant | Indole-4-carboxaldehyde | HCID 333703 | — |
| Product | 1-(4-Methyl-3-pentenyl)indole-4-carbaldehyde | HCID 18973551 | 86.9% |
Reaction Steps
The same procedures used in Example 7 were repeated except for using 4.59 g of 5-bromo-2-methyl-2-pentene and 2.00 g of indole-4-carbaldehyde as a starting material to give 2.72 g of 1-(4-methyl-3-pentenyl)indole-4-carbaldehyde as a brown oily substance. The yield thereof was found to be 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811439 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-81dbeea5ecfd4b8eb08457c4f13944f0 |
| Source note | uspto-grants-1998_09 |