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HRID 128848作成日:2026年10月27日

4,4'-Difluorobenzophenone → Phthalonitrile

https://huagongshe.com/reaction/128848

反応式

関与物質

役割名称HCID仕込み量
反応物4,4'-DifluorobenzophenoneHCID 9582—
反応物Potassium CarbonateHCID 11430—
反応物DimethylacetamideHCID 31374—
反応物1,2-Benzenedicarbonitrile, 4-nitro-HCID 97443—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物PhthalonitrileHCID 7042358.4%

反応条件

温度160 °C

反応手順

To a 100 ml, 3-necked flask equipped with a thermometer and a Dean-Stark trap was added 5.0 gm (22.9 mmol) of 4,4'-difluorobenzophenone, 11.56 gm (36.7 mmol) of bisphenol A6F, and 40 ml of dimethylacetamide (DMAC). After flushing the mixture for 30 minutes with dry nitrogen, 7.6 gm (55.1 mmol) of pulverized anhydrous potassium carbonate was added with stirring. The light pink reaction mixture was stirred at 90° C. for 1 hour. Toluene was added to the Dean-Stark trap and to the reaction vessel (4 ml). The reaction mixture was refluxed at 145°-150° C. for 10 hours. Water which formed as a by-product was removed by azeotropic distillation. The toluene was removed by distillation while heating to 160° C. Upon cooling to room temperature, 6.37 gm (36.8 mmol) of 4-nitrophthalonitrile was added. The temperature of reaction mixture was increased to 70° C. and held at this temperature for 16 hours (overnight). The temperature was further increased to 110° C. and held for 1 hour. The room temperature mixture was poured into 400 ml of water with stirring to break the precipitate into a powdery form. The solid precipitate was collected by suction filtration, washed exhaustively with water, and dried to afford 16.9 gm of oligomeric phthalonitrile monomer.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464926
出典データセットuspto-grants-1995_11
ORD IDord-5b7559a513a74b688e30f83037b3e886
出典メモuspto-grants-1995_11