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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542998생성일: 2026년 10월 26일

p-Fluoronitrobenzene → 2-(2-Nitro-5-fluorophenyl)-1-phenylethanone

https://huagongshe.com/reaction/542998

반응식

참여 물질

역할이름HCID투입량
반응물p-FluoronitrobenzeneHCID 9590—
반응물BromineHCID 24408—
반응물Benzene, [1-[(trimethylsilyl)oxy]ethenyl]-HCID 117406—
반응물Tris(dimethylamino)sulfonium difluorotrimethylsilicateHCID 9795567—
반응물Sodium BisulfiteHCID 23665763—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물2-(2-Nitro-5-fluorophenyl)-1-phenylethanoneHCID 13507910—

반응 조건

온도-78 °C

반응 단계

To a solution of 2.12 mL (20 mmol) of 4-fluoronitrobenzene and 4.12 mL (21 mmol) of [(1-phenyl-1-ethenyl)oxy]trimethylsilane in 30 mL of THF at -78° C. was added 5.502 g (20 mmol) of TASF dissolved in 6 mL of acetonitrile and 5 mL of THF. After stirring for 3 hrs at -78° C., 1.00 mL (19.50 mmol) of bromine in 5 mL of cyclohexane was added dropwise. After being stirred for 15 min at -78° C., the mixture was warmed to room temperature and stirred further for 30 min. Thirty mL of saturated sodium bisulfite was added, and the product was extracted into four 60 mL portions of ether. The organic phase was washed with saturated sodium chloride, dried, and concentrated. Chromatography on silica using 30% ether/hexanes yielded the expected product. The yield was 1.660 g (38%) of product, which was an oil. The product material was analyzed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04659862
출처 데이터셋uspto-grants-1987_04
ORD IDord-258a31efbc8647d9be31c4f55bf237f4
출처 메모uspto-grants-1987_04