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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895835Generated: October 25, 2026

Tetrachloro-p-hydroquinone → 1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene

https://huagongshe.com/reaction/895835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrachloro-p-hydroquinoneHCID 66603—
ReactantTetrafluorophthalonitrileHCID 74600—
ReactantPotassium FluorideHCID 522689—
SolventAcetonitrileHCID 6342—
Product1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzeneHCID 1133093784.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 500 ml 4-necked flask, were poured 71.15 g (355 mmol) of tetrafluorophthalonitrile, 2.16 g (37.1 mmol) of potassium fluoride and 210 g of acetonitrile, and resulting was heated to 80° C. This mixture was kept at 80° C. with stirring, and to this mixture were dropped 4.40 g (17.7 mmol) of tetrachlorohydroquinone in 200 ml of acetonitrile over 1 hour. After dropping, reaction was performed at 80° C. for 6 hours. The reaction solution was cooled, filtrated, and the resulting residue washed with 30 ml and 15 ml of acetonitrile. After the filtrate had been concentrated on an evaporator to remove the solvent, 62.34 g of tetrafluorophthalonitrile was removed under in vacuo. To this was poured 27 ml of toluene and reflux performed for 1 hour. After cooling, the residue was washed with 5 ml, 25 ml and 5 ml of toluene, respectively, and further 12 ml of deionized water for three times. Finally, by drying the residue at 70° C. in vacuo, 9.08 g of 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene were obtained (yield: 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916959B2
Source datasetuspto-grants-2005_07
ORD IDord-1221684185074235ab6ef124b2e9f4a4
Source noteuspto-grants-2005_07