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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463549Generated: October 26, 2026

P-Anisidine → 4-Methoxybenzenediazonium tetrafluoroborate

https://huagongshe.com/reaction/1463549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantNitrous AcidHCID 24529—
ReactantTetrafluoroboric acidHCID 28118—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Methoxybenzenediazonium tetrafluoroborateHCID 517233—

Reaction Steps

p-Anisidine (30.75 g, 0.25 mole) was dissolved in aqueous tetrafluoroboric acid (48%, 110 ml) in a 500 ml 3 necked flask fitted with mechanical stirring, and cooled to 0°-10° C. Sodium nitrite (17.5 g, 0.25 mole) was separately dissolved in water (34 ml) and the solution cooled to 5°-10° C., and was then added dropwise to the reaction mixture over 60 minutes. The reaction mixture was stirred for about 45 minutes at 0°-10° C., and then tested with starch-iodide paper for excess nitrous acid. Any excess nitrous acid was destroyed by adding a small amount (approx. 0.1 g.) of sulfamic acid. The precipitate was filtered, washed once with ice-cold water (about 30 ml), and then twice with methanol (20 ml each time). The product diazonium tetrafluoroborate was dried under vacuum at ambient temperature. Yield 45.4 g (about 82%). This could be purified by dissolving in minimum amount of acetone, and precipitating with ether, repeating this process three times. The final product was filtered, washed with ether (30 ml), and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300675
Source datasetuspto-grants-1994_04
ORD IDord-975f9b7fd5454c5da3433d567ba07d9e
Source noteuspto-grants-1994_04