HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → N-Cyclohexylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | N-cyclohexylideneaniline | HCID 315516 | — |
| Catalyst | Zinc Acetate | HCID 11192 | — |
| Product | N-Cyclohexylaniline | HCID 74567 | — |
Reaction Steps
Reaction was carried out by the use of the same apparatus and the same procedure as in Example 1 except that zinc acetate was not employed. In this case, a distilled aniline layer contained, as impurities, 200-350 ppm of cyclohexanol, 1300-2200 ppm of cyclohexanone, 70-130 ppm of cyclohexylideneaniline and 20 ppm or less of nitrobenzene, and the purity of the aniline was merely 99.68-99.80%. Furthermore, in the liquid phase in the reactor, N-cyclohexylaniline was formed rapidly and its content reached about 1.7% after 9 hours had elapsed since the start of the reaction, although the content of nitrobenzene in this liquid phase was maintained at 0.01% or less.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05283365 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-9616a9f5c7534990bc5573bcffaf83b7 |
| Source note | uspto-grants-1994_02 |