HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415194Generated: October 30, 2026
3-Hydroxyanthranilic Acid → HCID 66621013, compound
https://huagongshe.com/reaction/415194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxyanthranilic Acid | HCID 86 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Acetate | HCID 175 | — |
| Product | HCID 66621013 | HCID 66621013 | 47.2% |
Reaction Steps
To a suspension of 3-hydroxyanthranilic acid (0.153 g, 1.0 mmol) in toluene (10 mL) was added 4-bromobenzoyl chloride (0.603 g, 3.0 mmol) followed by pyridine (0.275 g, 3.5 mmol) at room temperature. The resulting mixture was stirred at room temperature for 30 minutes then heated to 80° C. for 1 hr. After this time the reaction was cooled and poured into a mixture of ethyl acetate (50 mL) and 5% aqueous hydrochloric acid (20 mL). Subsequent separation of the layers, drying the organic over anhydrous magnesium sulfate and filtration afforded a solution. After removal of the solvent, the residue was dissolved in toluene (20 mL) and the solution treated with 4-methylbenzenesulfonic acid (0.4 g, 2.1 mmol). The reaction mixture was then heated to reflux overnight. After this time the reaction was cooled and poured into water (100 mL), the organic layer was separated, washed with water (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to a solid. Re-crystallization of this solid from acetate gave 2-(4-bromophenyl)benzo[d]oxazole-4-carboxylic acid as a white solid (0.075 g, yield 24%). LC-MS (ESI) m/z 320 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08088760B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-4a8927d68c8349b69db96a4276d8ff0a |
|---|
| Source note | uspto-grants-2012_01 |
|---|