HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2Indenyl)indole → 6-Oxo carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2Indenyl)indole | HCID 10585619 | — |
| Reactant | Ethyl (2Z)-3-cyanoprop-2-enoate | HCID 15577688 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Diethylaluminum chloride | HCID 7277 | — |
| Solvent | Ethylaluminum dichloride | HCID 11237 | — |
| Solvent | Tin tetrachloride | HCID 24287 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Solvent | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 6-Oxo carbazole | HCID 18980403 | — |
Reaction Steps
In Method B (FIG. 2), a 2-(heteroaryl)indole derivative (1-3), or 2-(aryl)indole derivative such as 2-(2indenyl)indole 4 is reacted with ethyl cis-β-cyanoacrylate in the presence of a catalyst such as SnCl4, AlCl3, EtAlCl2, Et2AlCl or TFA in CH2 Cl2, C2H4Cl2 or toluene as solvent to give the 6-oxo carbazole compounds of formula I of the invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05801190 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-91e8c78440314a209782ee3b072a0f3c |
| Source note | uspto-grants-1998_09 |