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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279064생성일: 2026년 10월 26일

Nitrogen → (2-Fluoro-4-methylphenyl)boronic acid

https://huagongshe.com/reaction/279064

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Triethyl borateHCID 9009—
반응물4-Bromo-3-fluorotolueneHCID 573280—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물(2-Fluoro-4-methylphenyl)boronic acidHCID 2783132—

반응 조건

온도-70 °C

반응 단계

To a 500 mL three-necked round-bottomed flask equipped with septum and N2 inlet were added 10.0 g (52.9 mmol) 4-bromo-3-fluorotoluene and 100 mL dry tetrahydrofuran. The solution was cooled to −70° C., and 25.4 mL (63.5 mmol) of a 2.5 M solution of butyl lithium in hexane was added slowly so the temperature did not exceed −60° C. The clear solution was stirred at −70° C. for 1 hour, then treated with 10.8 mL (63.5 mmol) triethylborate. The reaction was stirred for 2 hours at −70° C., then warmed to room temperature and stirred for 16 hours. The reaction was quenched with saturated aqueous ammonium chloride solution, adjusted to pH 1-2 with 1 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and evaporated. The residue was triturated with hexane to a white solid, 6.1 g (75%), as a mixture of monoaryl and diaryl boronic acids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362195B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-3ce36dad2f7e49b88f501e441afa7a2a
출처 메모uspto-grants-2002_03