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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1060343Erstellt: 26. Oktober 2026

Sulfuric Acid → 2,3,5,6-Tetrafluoroaniline

https://huagongshe.com/reaction/1060343

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Edukt4-Amino-2,3,5,6-tetrafluorobenzonitrileHCID 87322—
Edukt2-AminotetrafluorobenzonitrileHCID 21731997—
Produkt2,3,5,6-TetrafluoroanilineHCID 12786—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

2,3,5,6-Tetrafluoroaniline was produced from 4-amino-2,3,5,6-tetrafluorobenzonitrile. To be specific, in a 200 ml four-neck flask provided with a stirrer, a thermometer, a dropping funnel, and a water separating tube, 100 g of 60% sulfuric acid was placed and heated to 140° C. To the hot sulfuric acid, 36 g of the raw material, 4-amino-2,3,5,6-tetrafluorobenzonitrile (having a purity of 94% and containing 6% of 2-amino-3,4,5,6-tetrafluorobenzonitrile as an impurity) was added dropwise at a rate of 6 g/hr. The 2,3,5,6-tetrafluoroaniline which was formed by the reaction was expelled by azeotropy with water, guided into the water dropping tube, and separated from the water. The reaction was continued for six hours while the reaction vessel was supplied with the same amount of water as expelled by distillation. After the completion of the reaction, the conversion ratio of the raw material determined by gas chromatography was found to be 96 mol %. When the 2,3,5,6-tetrafluoroaniline expelled by distillation was analyzed, the purity was found to be 95.3% and the yield to be 82.5%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06521794B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-c82e6f67570b4988be1a3777a2109457
Quellennotizuspto-grants-2003_02