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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415194Generated: October 30, 2026

3-Hydroxyanthranilic Acid → HCID 66621013, compound

https://huagongshe.com/reaction/415194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxyanthranilic AcidHCID 86—
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-Bromobenzoyl chlorideHCID 68515—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductAcetateHCID 175—
ProductHCID 66621013HCID 6662101347.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-4a8927d68c8349b69db96a4276d8ff0a
Source noteuspto-grants-2012_01