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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 371340Erstellt: 24. Oktober 2026

Hydrochloric Acid → Benzenediazonium tetrafluoroborate

https://huagongshe.com/de/reaction/371340

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAnilineHCID 6115—
EduktSodium TetrafluoroborateHCID 4343483—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
ProduktBenzenediazonium tetrafluoroborateHCID 5284485—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a 400 mL beaker containing 30 mL of concentrated hydrochloric acid and 30 mL of water was dissolved 9.2 g (0.1 mole) of aniline. The mixture was cooled to about 0° C. in an ice bath and then diazotized by the addition of a solution containing 7 g (0.1 mole) of sodium nitrite in 12 mL of water. After filtering, the solution was added slowly with stirring to 17 g (0.15 mole) of sodium fluoroborate (NaBF4) dissolved in 30 mL of water at room temperature (although lower temperatures can be used). After stirring another 5 minutes a white precipitate formed which was recovered by filtration, washed with 50 mL of cold water and 50 mL of diethyl ether and dried in vacuum. The yield of benzenediazonium tetrafluoroborate was about 75% of theory. The process (including a final thermal decomposition of the product, which is not employed in this Example), is commonly referred to as the Schiemann method. Kirk-Othmer, Encyclopedia of Chemical Technology, Second Edition, Vol. 9, page 568, Interscience (1966) describes this preparation and shows the equation including the decomposition as follows: ##STR2## A reference to this method is given in U.S. Pat. No. 3,950,444, column 1, lines 29-37, the disclosure of which is hereby incorporated by reference.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04530982
Quelldatensatzuspto-grants-1985_07
ORD IDord-c8d700cae8d44c15a7cbee76a19b59eb
Quellennotizuspto-grants-1985_07