HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,6-Dimethylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | 2,6-Dimethylphenol | HCID 11335 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,6-Dimethylaniline | HCID 6896 | — |
Reaction Steps
Hydroxy aromatics are aminated to form the corresponding aromatic amine by reaction at 200°-400°C with ammonia in the presence of a cyclohexanone and water in contact with a hydrogen transfer catalyst. For example, 2,6-dimethylphenol reacts with ammonia in the presence of cyclohexanone, water and a supported palladium catalyst to form 2,6-dimethylaniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931298 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-941b3fa9ac8e4911ae94a6a7963d6207 |
| Source note | uspto-grants-1976_01 |