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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28606생성일: 2026년 10월 24일

Hydrochloric Acid → 5-Chloro-2-(2,2,2-trifluoro-ethoxy)-phenylboronic acid

https://huagongshe.com/ko/reaction/28606

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Trimethyl borateHCID 8470—
반응물2-Bromo-4-chloro-1-(2,2,2-trifluoroethoxy)-benzeneHCID 22571484—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물5-Chloro-2-(2,2,2-trifluoro-ethoxy)-phenylboronic acidHCID 6898528061%

반응 조건

온도-70 °C

반응 단계

To a mixture of 2-bromo-4-chloro-1-(2,2,2-trifluoro-ethoxy)-benzene (3.0 g, 10.4 mmol) and tetrahydrofuran (60 ml), cooled to −70° C., was added a solution of isopropylmagnesium chloride in tetrahydrofuran (2 M, 5.7 ml). After warming to 0° C., the mixture was stirred for 1 hour. After cooling to −70° C., the mixture was treated with trimethylborate (1.2 g, 11.4 mmol). After stirring at room temperature for 12 hours, the mixture was treated with hydrochloric acid (2 M, 20 ml). After stirring for 40 minutes, the mixture was extracted with ethyl acetate (2×50 ml). The combined extracts were dried over magnesium sulfate and concentrated under reduced pressure. The residue was triturated with hexane (50 ml). Filtration and drying of the solid under reduced pressure gave 5-chloro-2-(2,2,2-trifluoro-ethoxy)-phenylboronic acid (1.6 g, 61% yield). 1H NMR (acetone-d6) δ 4.86 (q, 2H, J=8.5 Hz, CH2), 7.12 (d, 2H, J=4.6 Hz, OH), 7.20 (d, 1H, J=8.8 Hz, Ar), 7.49 (dd, 1H, J=8.8 Hz, J=2.8 Hz, Ar), 7.76 (d, 1H, J—2.7 Hz, Ar).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419984B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-abfc7fff02714648a50487ff850dc82a
출처 메모uspto-grants-2008_09