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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33962생성일: 2026년 10월 23일

Hydrogen Peroxide → 4-Bromoanisole

https://huagongshe.com/ko/reaction/33962

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Trimethyl borateHCID 8470—
반응물2,4-DibromoanisoleHCID 27011—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물4-BromoanisoleHCID 7730—

반응 조건

온도-78 °C

반응 단계

In a 500 mL round bottom flask was charged 2,4-dibromoanisole (5.0 g, 18.8 mmol) followed by 200 mL of dry tetrahydrofuran under nitrogen. The reaction mixture was then cooled to −78° C., and n-butyllithium (16.11 mL, 22.56 mmol) was added dropwise. The reaction mixture was stirred for 30 min at −78° C. The reaction mixture was then warmed to 0° C. and trimethylborate (2.57 mL, 22.56 mmol) was added dropwise. The reaction mixture was stirred at room temperature for 30 min. 5 mL of glacial acetic acid was added followed by 10 mL of 35% wt. hydrogen peroxide in a drop wise fashion. The reaction was allowed to stir 12 h at room temperature. The reaction was quenched with 1 N HCl, extracted with ethylacetate (100×3) and the combined organic phases were dried over Na2SO4, filtered and evaporated under reduced pressure. Purification by column chromatography yielded 1 g (26%) of 3-hydroxy, 4-methoxybromobenzene (white crystals). (96:4 Hexanes:ethylacetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429681B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-aafb1838a2e14327b1d6510484a2662a
출처 메모uspto-grants-2008_09