HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → N-(2-aminophenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(2-aminophenyl)benzamide | HCID 759408 | 59.8% |
Reaction Steps
1.62 g (10 mmole) of N,N′-carbonyldiimidazole were added to a dimethyl sulfoxide (10 ml) solution including 1.12 g (10 mmole) of benzoic acid, followed by stirring at room temperature for 1 hour. After the addition of 2.16 g (20 mmole, 2 equivalents) of 1,2-phenylenediamine, 1.9 ml of trifluoroacetic acid were added dropwise at room temperature. After reaction had been further carried out at room temperature for 15 hours, a post-treatment was performed in the same manner as in Example 6 to obtain 1.27 g (yield: 59%) of N-(2-aminophenyl)benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06320078B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-18f931a5b2e64e3eba60a5611f30c625 |
| Source note | uspto-grants-2001_11 |