HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluidine → 3H-Indole, 2,3,3,5-tetramethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Product | 3H-Indole, 2,3,3,5-tetramethyl- | HCID 117693 | 87% |
Reaction Steps
p-Toluidine was reacted with methyl isopropyl ketone in the same way as in Example 3. 2,3,3,5-Tetramethyl-3-H-indole 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-ea29e89ed2624bb29e83ff94ce698a23 |
| Source note | uspto-grants-1993_01 |