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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 415133Erstellt: 24. Oktober 2026

3-Hydroxyanthranilic Acid → 2-p-Tolylbenzoxazole-4-carboxylic acid

https://huagongshe.com/de/reaction/415133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Hydroxyanthranilic AcidHCID 86—
EduktHydrochloric AcidHCID 313—
EduktPyridineHCID 1049—
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt4-Methylbenzoyl ChlorideHCID 13405—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-p-Tolylbenzoxazole-4-carboxylic acidHCID 6662130860%

Reaktionsschritte

To a suspension of 3-hydroxyanthranilic acid (0.153 g, 1 mmol) in toluene (10 mL) was added 4-methylbenzoylchloride (0.464 g, 3 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 80C 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 MgSO4 and filtration afforded a solution. After removal of the solvent, the residue was dissolved in xylenes (20 mL) and the solution treated with p-TsOH (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 separated then washed with water (100 mL). The organic was dried over MgSO4, filtered and concentrated to a solid. Recrystallization of this solid from ethyl acetate gave a white solid product, 2-p-tolylbenzo[d]oxazole-4-carboxylic acid (0.15 g, 60% yield). MS (ESI) m/e 254 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088760B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-077aa96292b24018a811234f39f85d07
Quellennotizuspto-grants-2012_01