Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylbenzene | HCID 7500 | — |
| Reactant | Tetrafluoroterephthalonitrile | HCID 15783 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 2,3,5,6-Tetrafluorobenzonitrile | HCID 297546 | — |
Reaction Steps
200 g of ethylbenzene, 0.30 g of 5% palladium/activated carbon, and 6.0 g of 2,3,5,6-tetrafluoroterephthalonitrile were added to a 1000 cc stainless steel autoclave in a nitrogen atmosphere. The gas phase was sufficiently replaced with a mixed gas of 41 vol % hydrogen and 59 vol % nitrogen, then the mixed gas was used to keep the pressure at 0.23 MPa and the temperature was maintained at 190° C. After 2, 4, and 6 hours, the reaction solution was analyzed by gas chromatography, whereupon the conversions of 2,3,5,6-tetrafluoroterephthalonitrile were found to be 23, 62, and 99% and the yields of 2,3,5,6-tetrafluorobenzonitrile (based on 2,3,5,6-tetrafluoroterephthalonitrile) were 22, 56, and 87%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06020517 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-73e1ffea1a3f4f058791095336063d70 |
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| Source note | uspto-grants-2000_02 |
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