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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2249387생성일: 2026년 10월 24일

Methyl iodide → 1-Bromo-2,4-difluoro-5-methoxybenzene

https://huagongshe.com/ko/reaction/2249387

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Peracetic AcidHCID 6585—
반응물Trimethyl borateHCID 8470—
반응물Potassium CarbonateHCID 11430—
반응물1,5-Dibromo-2,4-difluorobenzeneHCID 10564511—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물1-Bromo-2,4-difluoro-5-methoxybenzeneHCID 6880937923.2%

반응 조건

온도0 °C

반응 단계

To a solution of 1,3 dibromo-4,6-difluorobenzene (10.0 g, 37 mmol) in THF (50 mL) at −20° C. was added isopropyl magnesium chloride (2.0M in THF, 42 mmol) and the resulting solution warm to 0° C. and stirred for 30 minutes. Trimethylborate (4.7 g, 45 mmol) was added and the mixture stirred at ambient temperature for 1 hour. The solution was recooled to −20° C. and peracetic acid (32%, 50 mmol) was added and the solution was stirred for 30 minutes at ambient temperature. The solution was then quenched with sodium bisulfite (5% solution, 75 mL) and then acidified with 6 N hydrochloric acid and extracted with ethyl ether (2×75 mL). Combined extracts were dried (sodium sulfate) and concentrated. The crude phenol was dissolved in acetonitrile (40 mL) and potassium carbonate (10 g, 74 mmol) and iodomethane (5.7 g, 40 mmol) were added and stirred at ambient temperature for 20 hours. The solution was concentrated and the residue taken into water (50 mL) and extracted with ethyl ether (2×75 mL) and the combined extracts were washed with brine, dried (sodium sulfate), and concentrated. The residue was purified by chromatography (hexanes) to give 1-bromo-2,4-difluoro-5-methoxybenzene (2.0 g, 8.6 mmol): LC/MS (m/z=223).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07314849B2
출처 데이터셋uspto-grants-2008_01
ORD IDord-1e80e3bf6ab845a7a23530927ed62f13
출처 메모uspto-grants-2008_01