Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 15538104 | HCID 15538104 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15538105 | HCID 15538105 | — |
Reaction Steps
To Diphenylphosphoryl azide (5.75 g) in anhydrous toluene (50 mL) al. 100° C. under nitrogen was added dropwise a solution containing Ethyl-3-nitro-4-carboxybenzoate (5 g) and triethylamine (4 mL) in anhydrous toluene (50 mL). The mixture was stirred for 1 h followed by the addition of aniline (5 mL). and the reaction was allowed to cool to room temperature (40 min). Ethyl acetate (300 mL) was added and the solution was washed successively with 1N HCl (300 mL), water (300 mL), 1N NaOH (300 mL) and water (300 mL). The organic layer was dried and the solvent was removed ill vacuo. To the resulting oil was added diethyl ether (50 mL). and the resulting solid was collected and dried yielding N-(2-Nitro-5-methylphenyl)-N′-phenyl-urea as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06268496B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-82f12b1fcfa1445891c8a7e0c85b744c |
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| Source note | uspto-grants-2001_07 |
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