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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1397476생성일: 2026년 10월 26일

Hydrogen Peroxide → N-(4-bromo-2-fluorophenyl)-5,7-dimethylbenzo[d]oxazol-2-amine

https://huagongshe.com/reaction/1397476

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물6-Amino-2,4-xylenolHCID 100530—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물4-Bromo-2-fluorophenylisothiocyanateHCID 2757003—
용매TetrahydrofuranHCID 8028—
생성물N-(4-bromo-2-fluorophenyl)-5,7-dimethylbenzo[d]oxazol-2-amineHCID 22347267—

반응 단계

An ambient solution of 2-amino-4,6-dimethylphenol (0.85 g, 6.2 mmol) and 2-fluoro-4-bromophenyl isothiocyanate (1.44 g, 6.20 mmol) in tetrahydrofuran (20 mL) was stirred for 16 h. The reaction was cooled (0° C.), and LiOH.H2O (0.521 g, 12.41 mmol) was added, followed by the dropwise addition of 30% H2O2 (3.41 mL, 31.0 mmol) over 15 minutes. The reaction was warmed to room temperature and stirred for 16 h. The reaction was then quenched by the addition of 20% aqueous sodium sulfite; solution (50 mL) and ethyl acetate (75 mL). The layers were separated, and the aqueous was extracted with additional ethyl acetate (2×75 mL). The combined organics were dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by chromatography on SiO2 gel, eluting with 25% ethyl acetate in hexane, to give the title compound. MS (ESI) m/z 335 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901152B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-3aeac27d846d4e9c99049251a98b0cc6
출처 메모uspto-grants-2014_12