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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341703생성일: 2026년 10월 25일

Hydrochloric Acid → (4-Bromo-2,6-dimethylphenyl)boronic acid

https://huagongshe.com/reaction/341703

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Trimethyl borateHCID 8470—
반응물5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(4-Bromo-2,6-dimethylphenyl)boronic acidHCID 5749730143.7%

반응 조건

온도-75 °C

반응 단계

To a solution of 4-bromo-2,6-dimethyl-1-iodobenzene (150 g, 0.48 mol) in tetrahydrofuran (1500 ml) at −75° C. is added n-butyl lithium (1.6 M in hexanes, 364 ml, 0.58 mol) dropwise maintaining the temperature of the reaction mixture below −70° C. When the addition is complete the mixture is stirred at −75° C. for an additional 30 minutes and then trimethyl borate (302 g, 2.9 mol) is added dropwise. After the addition is complete the reaction is stirred at −75° C. for 1 hour, then allowed to come to room temperature and stirred for 2 hours, followed by cooling in an ice bath and acidification with 0.5 N aqueous hydrochloric acid. The mixture is extracted with ethyl acetate (3×1000 ml) and the organic extracts are combined, washed with brine, dried over anhydrous sodium sulphate. The mixture is filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-bromo-2,6-dimethylphenylboronic acid (48 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-c6a1d681e830422eb8e2f8b1d14f81ac
출처 메모uspto-grants-2014_11