HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl N-phenylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Carbon tetraiodide | HCID 10487 | — |
| Reactant | Rubidium hydroxide | HCID 62393 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Product | Ethyl N-phenylcarbamate | HCID 7591 | — |
Reaction Steps
In a 200 ml stirring type autoclave were charged 30 mmols of aniline, 15 mmols of nitrobenzene, 50 ml of ethanol, 3 mmols of palladium chloride, 3 mmols of tetraiodomethane and 3 mmols of rubidium hydroxide. After the air inside the autoclave had been replaced with carbon monoxide, carbon monoxide was pressurized into the autoclave to 120 Kg/cm2, and the reaction was carried out at 180° C. for 5 hours with stirring. As the result of analysis of the reaction solution, the conversions of aniline and nitrobenzene were 21% and 29%, respectively, and 8 mmols of ethyl N-phenylcarbamate were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04621149 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-fa798d41ff08449c9a5db5ad96fd995c |
| Source note | uspto-grants-1986_11 |