Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | N-Methylaniline | HCID 7515 | — |
| Product | Aniline | HCID 6115 | — |
| Product | Nitrobenzene | HCID 7416 | — |
| Product | N-Methylenebenzenamine | HCID 66014 | — |
Reaction Steps
The procedure was the same as for Example 1 with the exception that aniline was omitted from the initial reaction solution. As the reactor contents heated to 160° C., approximately 30% of the nitrobenzene was converted. Complete nitrobenzene conversion required 5.5 hours at 160° C. and yielded 0.068 mole methyl N-phenyl carbamate (68% selectivity), 0.022 mole aniline, 0.007 mole N-methylene aniline, and 0.001 mole (N-methylaniline (summed to 30% selectivity to aniline).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04687872 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-c57a0c1cee394dc3b25d45365e2a55ac |
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| Source note | uspto-grants-1987_08 |
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