HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzoic Acid → 4-[(3-Methyl-1,2-oxazole-5-carbonyl)amino]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methyl-1,2-oxazole-5-carbonyl chloride | HCID 12905099 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-[(3-Methyl-1,2-oxazole-5-carbonyl)amino]benzoic acid | HCID 21432227 | 73.7% |
Reaction Steps
To a stirred suspension of 6.9g of p-aminobenzoic acid and 3.5 g of potassium carbonate in 60 ml of acetone was added 7.3 g of 3-methylisoxazole-5-carbonyl chloride. The mixture was stirred at room temperature for 1 hr. and then refluxed for 1 hr. The precipitate was filtered off and dissolved in water. The solution was acidified with concentrated hydrochloride acid. The precipitate was filtered off and washed with ethanol. There was obtained 9.1 g of N-(p-carboxyphenyl)-3-methylisoxazole-5-carboxamide. Melting point: above 300° C. Yield: 73.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026902 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-3ef31d1a859c46f79597e24cc5a20b64 |
| Source note | uspto-grants-1977_05 |