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HRID 358807作成日:2026年10月26日

4-Bromo-2-fluoroanisole → 3-Fluoro-4-methoxybenzonitrile

https://huagongshe.com/reaction/358807

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-2-fluoroanisoleHCID 75378—
反応物HCID 178418260HCID 178418260—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-Fluoro-4-methoxybenzonitrileHCID 277454878%

反応手順

20 g of the 2-fluoro-4-bromoanisole thus obtained and 9.8 g of copper cyanide were dissolved in 100 ml of dimethyl formamide and heated under reflux for ten hours. To the reaction mixture, was added an aqueous solution of 20 g of ferric chloride in 100 ml of water. The reaction mixture was allowed to cool to room temperature and the reaction product was extracted with toluene. The organic layer was successively washed with water, a saturated aqueous solution of sodium carbonate and a saturated aqueous solution of common salt. Then the organic layer was separated. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate 10:1) and further recrystallized from ethanol. Thus 10.0 g of 3-fluoro-4-methoxybenzonitrile was obtained. Yield: 68%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04997942
出典データセットuspto-grants-1991_03
ORD IDord-d3fc8bc045b6442b88e625d098ce7d2f
出典メモuspto-grants-1991_03