HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Product | Aniline | HCID 6115 | — |
| Product | Ethyl N-phenylcarbamate | HCID 7591 | — |
Reaction Steps
The procedure was the same as for Example 2 with the exception that ethanol was substituted for methanol on an equal volume basis. Complete conversion of the nitrobenzene occurred in 4.5 hours at 160° C. and yielded 0.014 mole ethyl N-phenylcarbamate, and 0.058 mole additional aniline (0.108 mole total aniline). The balance (0.023 mole) appeared as by-products derived from aniline. It is thus clear that the selectivity of the ruthenium catalyzed conversion of nitrobenzene and methanol to methyl N-phenylcarbamate is higher than the selectivity of the corresponding conversion of nitrobenzene and ethanol to ethyl N-phenylcarbamate even when aniline is added in order to improve the selectivity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629804 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-e2c27a1c03ca47d8b5e8ec729f86e02e |
| Source note | uspto-grants-1986_12 |