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HRID 415133作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-Hydroxyanthranilic AcidHCID 86—
反応物Hydrochloric AcidHCID 313—
反応物PyridineHCID 1049—
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-Methylbenzoyl ChlorideHCID 13405—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-p-Tolylbenzoxazole-4-carboxylic acidHCID 6662130860%

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088760B2
出典データセットuspto-grants-2012_01
ORD IDord-077aa96292b24018a811234f39f85d07
出典メモuspto-grants-2012_01