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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371340Generated: October 25, 2026

Hydrochloric Acid → Benzenediazonium tetrafluoroborate

https://huagongshe.com/reaction/371340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
ReactantSodium TetrafluoroborateHCID 4343483—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductBenzenediazonium tetrafluoroborateHCID 5284485—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04530982
Source datasetuspto-grants-1985_07
ORD IDord-c8d700cae8d44c15a7cbee76a19b59eb
Source noteuspto-grants-1985_07