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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7706생성일: 2026년 10월 23일

2-Aminophenol → 5-(1,3-Benzoxazol-2-yl)-2-methylphenol

https://huagongshe.com/ko/reaction/7706

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물p-Toluenesulfonic acidHCID 6101—
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물3-Hydroxy-4-methylbenzoic acidHCID 68512—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-(1,3-Benzoxazol-2-yl)-2-methylphenolHCID 21991000—

반응 단계

To a 100 mL round-bottom flask with 3-hydroxy-4-methylbenzoic acid (2.5 g, 16.4 mmol), was added dropwise SOCl2 (15 mL). The reaction was refluxed for 30 min and cooled to rt. The excess of SOCl2 was removed in vacuo and the oily acid chloride was dissolved in THF (15 mL). This resulting solution was added dropwise to a mixture of 2-aminophenol (1.8 g, 16.4 mmol), triethylamine (1.7 g, 16.4 mmol) and THF (30 mL) at 0° C. The resulting reaction mixture was then brought to rt for 30 min and the resulting precipitate was removed by filtration. The filtrate was concentrated and dried under vacuum. The resulting dark brown solid residue was dissolved in toluene (20 mL) and p-toluenesulfonic acid (15.6 g, 82 mmol) was added. The reaction was refluxed overnight, cooled at rt and EtOAc (500 mL) was added. The EtOAc solution was washed with brine (3×50 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was recrystallized in EtOAc to afford 5-(1,3-benzoxazol-2-yl)-2-methylphenol as a light yellow solid. MS (ESI) 226 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-bde3b58972f64cb4a1179033e865bdef
출처 메모uspto-grants-2006_08