Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | HCID 67237480 | HCID 67237480 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 57625605 | HCID 57625605 | — |
Reaction Steps
A suspension of 4-nitroanthranilic acid isobutyramide (4 g, 15.8 mmol), 4-chloroaniline (2.2 g, 17.2 mmol) and phosphorus trichloride (5.6 mL) in toluene (150 mL) is heated to reflux (bath temperature for 150° C.) for 2 hours. The reaction mixture is allowed to cool to room temperature and then evaporated to dryness. The residue is partitioned between water and EtOAc and the aqueous phase is extracted (2×) with EtOAc. The combined organic phases are washed with water, dried (Na2SO4) and evaporated in vacuo. Trituration with isopropyl ether provides the desired compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102653B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-cba5ed846ff442358c2d71858667f57a |
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| Source note | uspto-grants-2015_08 |
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