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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415133생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물3-Hydroxyanthranilic AcidHCID 86—
반응물Hydrochloric AcidHCID 313—
반응물PyridineHCID 1049—
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-Methylbenzoyl ChlorideHCID 13405—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-p-Tolylbenzoxazole-4-carboxylic acidHCID 6662130860%

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088760B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-077aa96292b24018a811234f39f85d07
출처 메모uspto-grants-2012_01