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HRID 373741作成日:2026年10月26日

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

https://huagongshe.com/reaction/373741

反応式

関与物質

役割名称HCID仕込み量
反応物p-FluoronitrobenzeneHCID 9590—
反応物BromineHCID 24408—
反応物Benzene, [1-[(trimethylsilyl)oxy]ethenyl]-HCID 117406—
反応物Tris(dimethylamino)sulfonium difluorotrimethylsilicateHCID 9795567—
反応物Sodium BisulfiteHCID 23665763—
溶媒AcetonitrileHCID 6342—
溶媒TetrahydrofuranHCID 8028—
溶媒CyclohexaneHCID 8078—
生成物2-(2-Nitro-5-fluorophenyl)-1-phenylethanoneHCID 13507910—

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05164499
出典データセットuspto-grants-1992_11
ORD IDord-094239ba94bc4dcca939ac2ca53597b2
出典メモuspto-grants-1992_11