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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1599182Erstellt: 27. Oktober 2026

Carbon Dioxide → 1,2,3,4-Tetrafluorobenzene

https://huagongshe.com/reaction/1599182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktSodium HydroxideHCID 14798—
Edukt2,3,4,5-Tetrafluorobenzoic acidHCID 297549—
KatalysatorHCID 178419072HCID 178419072—
LösungsmittelWaterHCID 962—
Produkt1,2,3,4-TetrafluorobenzeneHCID 11084—

Reaktionsschritte

19.4 g (0.1 mol) of 2,3,4,5-tetrafluorobenzoic acid are dissolved in 40 g of water, 20 g of a mixture of trialkylamines having 6 to 14 carbon atoms (Hostarex A 327; a commercial product of Hoechst AG) and 0.2 g of copper(I) oxide are added and the pH is adjusted to 7 by addition of 30% strength aqueous sodium hydroxide solution. The decarboxylation is carried out in an autoclave at 155° C. within a period of 4 hours, the evolved carbon dioxide at a pressure of 12 bar being depressurized via a pressure cooler and the distillate passing overhead in this case being collected (cold trap -78° C.). After termination of the reaction, the autoclave is cooled and the 1,2,3,4-tetrafluorobenzene is distilled off by steam at 100° C. and 1.5 l of distillate are obtained, which distillate is combined with the distillate collected previously. The combined distillates are extracted by means of dichloromethane, the organic phase is separated off, dried over magnesium sulfate, filtered and the solvent is removed in vacuo. 10.5 g of crude, slightly yellowish 1,2,3,4-tetrafluorobenzene are obtained, which can be brought to a very high purity by fractional distillation.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05739388
Quelldatensatzuspto-grants-1998_04
ORD IDord-11e936efbc214e6493ffbbc303c0ee81
Quellennotizuspto-grants-1998_04