HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 1,2,3,4-Tetrahydrocarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Product | 1,2,3,4-Tetrahydrocarbazole | HCID 13664 | 87% |
Reaction Steps
Aniline was reacted with cyclohexanone in the same way as in Example 3. Tetrahydrocarbazole was formed in a yield of 87% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179211 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-bcb663bf6d44472aad6c1506f0936c16 |
| Source note | uspto-grants-1993_01 |