Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | HCID 21202665 | HCID 21202665 | — |
| Product | Carbanilide | HCID 7595 | — |
Reaction Steps
The experiment as described in Example 10 was repeated at a temperature of 110° C. using nitrobenzene (7.5 ml) and aniline (4 ml) as feed. Gas-liquid chromatography indicated that the initial amount of aniline had been converted completely and that 1,3-diphenylurea had been formed in high yield (90%, based on aniline. Methyl carbanilate had been obtained in 60% yield, based on nitrobenzene with a nitrobenzene conversion of about 70%). The reaction temperature was then raised to 135° C. and the reaction was allowed to proceed at that temperature for another 5 hours. The total conversion of nitrobenzene amounted to 90% and more methylcarbanilate had been formed, corresponding to the amount of 1,3-diphenylurea converted.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474978 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-0076306968364dfb864614e5c064482d |
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| Source note | uspto-grants-1984_10 |
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