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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34021생성일: 2026년 10월 25일

Dimethylformamide → 5-Bromo-2,3-difluoro-4-(trimethylsilyl)benzaldehyde

https://huagongshe.com/reaction/34021

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물DiisopropylamineHCID 7912—
반응물(6-Bromo-2,3-difluorophenyl)trimethylsilaneHCID 23070109—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물5-Bromo-2,3-difluoro-4-(trimethylsilyl)benzaldehydeHCID 23070176—

반응 조건

온도-78 °C

반응 단계

Under nitrogen atmosphere, to a solution containing 6.34 mL of N,N-diisopropylamine in 100 mL of tetrahydrofuran, 26.4 mL of 1.57 Mn-butyllithium in hexane was added at 0° C., and stirred at this temperature for 10 minutes. After cooling to −78° C., a solution containing 10.0 g of (6-bromo-2,3-difluorophenyl)trimethylsilane in 100 mL of tetrahydrofuran was added dropwise, stirred at this temperature for 1 hour, then added dropwise with 2.92 mL of N,N-dimethylformamide, allowed to gradually warm to room temperature, and stirred fro 3 hours. After diluting with water and ethyl acetate, the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (n-hexane), to afford 9.70 g of the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429609B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ffc56b65863d460a9838b0858a75ec3d
출처 메모uspto-grants-2008_09