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HRID 128849作成日:2026年10月25日

4,4'-Difluorobenzophenone → Phthalonitrile

https://huagongshe.com/reaction/128849

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 7042501.4%

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, 8.03 gm (23.9 mmol) of bisphenol A6F, and 50 ml of dimethylacetamide (DMAC). After flushing the mixture for 30 minutes with dry nitrogen, 3.9 gm (28.7 mmol) of pulverized anhydrous potassium carbonate was added with stirring. The reaction mixture was stirred at 70° 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 24 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 50° C., 3.10 gm (17.9 mmol) of 4-nitrophthalonitrile was added. Since the reaction mixture was somewhat viscous, the temperature of the mixture was increased to 110° C. and held at this temperature for 18 hours (overnight). FTIR spectroscopy showed the absence of hydroxy and nitro bands. The room temperature mixture was then poured into 300 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 11.5 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-1d68e98a815848f2ac1359ef9e680312
出典メモuspto-grants-1995_11