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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1161587생성일: 2026년 10월 24일

Hydrogen Peroxide → 5-Ethoxy-2-fluorophenol

https://huagongshe.com/ko/reaction/1161587

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Trimethyl borateHCID 8470—
반응물Sodium SulfiteHCID 24437—
반응물4-FluorophenetoleHCID 68018—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물5-Ethoxy-2-fluorophenolHCID 18003370—

반응 단계

To 150 ml of a THF solution containing 10.5 g of 1-ethoxy-4-fluorobenzene, 50 ml of n-butyllithium (1.58 M, hexane solution) was added dropwise at −78° C. under a nitrogen atmosphere. The resulting mixture was stirred for 4 and a half hours, then 8.9 ml of trimethoxy boron was added thereto. Then, the temperature of the mixture was slowly allowed to rise to room temperature. The reaction mixture was stirred for 3 and a half hours, then 12.9 ml of acetic acid and 12.7 ml of a 30% hydrogen peroxide aqueous solution were added thereto at 0° C. The mixture was stirred at room temperature overnight, and then a saturated sodium sulfite aqueous solution was added thereto. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The desiccating agent was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was crudely purified by silica gel column chromatography (ethyl acetate-heptane) to give a crude product of 5-ethoxy-2-fluorophenol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07816522B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-6e9c26d66c1f48aa988ae9b63bf1027d
출처 메모uspto-grants-2010_10