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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128848Generated: October 26, 2026

4,4'-Difluorobenzophenone → Phthalonitrile

https://huagongshe.com/reaction/128848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4'-DifluorobenzophenoneHCID 9582—
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylacetamideHCID 31374—
Reactant1,2-Benzenedicarbonitrile, 4-nitro-HCID 97443—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductPhthalonitrileHCID 7042358.4%

Reaction Conditions

Temperature160 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464926
Source datasetuspto-grants-1995_11
ORD IDord-5b7559a513a74b688e30f83037b3e886
Source noteuspto-grants-1995_11