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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 885104생성일: 2026년 10월 25일

Hydrogen Peroxide → N-(4-bromophenyl)-7-methylbenzo[d]oxazol-2-amine

https://huagongshe.com/reaction/885104

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물4-Bromophenyl isothiocyanateHCID 16133—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물6-Amino-o-cresolHCID 413657—
용매TetrahydrofuranHCID 8028—
생성물N-(4-bromophenyl)-7-methylbenzo[d]oxazol-2-amineHCID 68721392—

반응 단계

An ambient solution of 2-amino-6-methylphenol (0.74 g, 6.0 mmol) and 4-bromophenyl isothiocyanate (1.28 g, 6.0 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 303[M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242139B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-61d75497f0f546a1bf1372e3cd63836b
출처 메모uspto-grants-2012_08