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 | — |
| Product | N-Ethylaniline | HCID 7670 | — |
| Product | N-Ethylideneaniline | HCID 95796 | — |
Reaction Steps
The procedure was the same as for Example 1 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 0.007 mole ethyl N-phenylcarbamate, 0.066 mole aniline, 0.004 mole ethylidene aniline, and 0.002 mole N-ethyl aniline. The balance (0.021 mole) was converted to higher molecular weight products derived from aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629804 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-52e124886b6440d1930d86865a2807af |
| Source note | uspto-grants-1986_12 |