HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Methyl phenylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Carbanilide | HCID 7595 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Potassium | HCID 5462222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl phenylcarbamate | HCID 17451 | — |
Reaction Steps
In a 200 ml stirring type autoclave were charged 30 mmols of N,N'-diphenylurea, 15 mmols of nitrobenzene, 50 ml of methanol, 1 mmol of potassium tetrabromopalladate, 2 mmols of iodine and 2 mmols of triethylamine. 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 6 hours with stirring. As the result of analysis of the reaction solution, the conversions of N,N'-diphenylurea and nitrobenzene were 30% and 38%, respectively, and 15 mmols of methyl 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-de11fa3b8cac42f689442ceea5846ca8 |
| Source note | uspto-grants-1986_11 |