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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7708생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/7708

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 SOCl2 (15 mL) dropwise. The reaction was refluxed for 30 min, cooled to rt and the excess of SOCl2 was removed in vacuo. The oily acid chloride was dissolved in THF (15 mL) and the 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 reaction was then warmed to rt for 1 h and the precipitate was removed by filtration. The filtrate was concentrated and dried in vacuo and the 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 to rt and dissolved in EtOAc (500 mL). The organic 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-10019520ef6f48319b08b25838da63f4
출처 메모uspto-grants-2006_08