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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 376514Erstellt: 25. Oktober 2026

Ethylbenzene → 2-Phenylpropionitrile

https://huagongshe.com/reaction/376514

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylbenzeneHCID 7500—
EduktTetrafluoroterephthalonitrileHCID 15783—
Edukt2,3,5,6-TetrafluorobenzonitrileHCID 297546—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
Produkt2-PhenylpropionitrileHCID 15761—

Reaktionsschritte

100 g of ethylbenzene and 3.0 g of 5% palladium/activated carbon were added to a 1000 cc stainless steel autoclave. The gas phase was sufficiently replaced with hydrogen gas, then hydrogen gas was used to apply a pressure of 0.3 MPa and make the temperature 100° C. and catalytic pretreatment was carried out for 1 hour. The gas phase was again sufficiently replaced with nitrogen, then 3.0 g of the reaction material, that is, 2,3,5,6-tetrafluoroterephthalonitrile was added. The nitrogen atmosphere was maintained, the autoclave sealed as it was at atmospheric pressure, and the temperature held at 175° C. After 3 hours, the reaction solution was analyzed by gas chromatography, whereupon the conversion of 2,3,5,6-tetrafluoroterephthalonitrile was found to be 100% and the yield of 2,3,5,6-tetrafluorobenzonitrile (based on 2,3,5,6-tetrafluoroterephthalonitrile) was 95%. At the same time, 13.4 mmol of α-methylbenzylcyanide was produced. This corresponded to 0.95 times molar amount relative to the production of 2,3,5,6-tetrafluorobenzonitrile.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06020517
Quelldatensatzuspto-grants-2000_02
ORD IDord-4362807adf114823bd7dabea1f3e1abb
Quellennotizuspto-grants-2000_02