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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851738Generated: November 2, 2026

Hydrochloric Acid → HCID 12524399, compound

https://huagongshe.com/reaction/1851738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-BromoanilineHCID 11992—
ReactantTetrafluoroboric acidHCID 28118—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 12524399HCID 1252439948%

Reaction Conditions

Temperature0 °C

Reaction Steps

9.5 mL of concentrated hydrochloric acid, 65 mL of pure water, and 6.0 g (35 mmol) of 2-bromoaniline were put into a 200 mL four-necked flask, and they were then dissolved by heating. The obtained solution was cooled to 0° C. Thereafter, an aqueous solution of 2.46 g (35.1 mmol) of sodium nitrite that had previously been dissolved in 7.5 mL of pure water was added dropwise thereto over approximately 10 minutes. The reaction solution that was first in a gruel-like state was converted to a light yellow transparent liquid by stirring for 30 minutes. Subsequently, 12.5 g (59.8 mmol) of a 42 mass % HBF4 aqueous solution was added dropwise thereto over approximately 5 minutes. As a result, light yellow crystals were immediately precipitated. The reaction solution was stirred for 30 minutes, and then the crystals were filtered through a glass filter. The resultant was washed with 30 mL of pure water, and was then washed with a mixed solution of 8 mL of methanol and 32 mL of ether. Thereafter, the resultant was dried under a reduced pressure, so as to obtain 4.5 g of 2-bromobenzenediazonium tetrafluoroborate (yield: 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957233B2
Source datasetuspto-grants-2015_02
ORD IDord-a01c469e239046ce8fc928c78f00157c
Source noteuspto-grants-2015_02