Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47906Generated: October 23, 2026

Hydrogen Bromide → 3-Cyano-2,4-dichloro-5-fluorobromobenzene

https://huagongshe.com/en/reaction/47906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantWaterHCID 962—
ReactantHydrate;hydrochlorideHCID 21885828—
Reactant3-Cyano-2,4-dichloro-5-fluoroanilineHCID 23431778—
ReactantSodium NitriteHCID 23668193—
Product3-Cyano-2,4-dichloro-5-fluorobromobenzeneHCID 2343179086.2%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

47.2 g of 3-cyano-2,4-dichloro-5-fluoroaniline (0.23 mol) were added to a solution of 150 ml of hydrochloric acid-water (1:1). The resulting mixture was stirred to be a slurry and then cooled to 0-5° C. A solution of sodium nitrite (16.7 g, 0.242 mol) and water (46 ml) was added thereto over 30 minutes. The resulting solution was added to a solution of cuprous bromide (0.275 mol) in 147 ml of hydrobromic acid. The reaction mixture was stirred for 2 hours and allowed overnight. The resulting mixture was wet-distilled. The distilled fraction was extracted with toluence. The oil layer was washed successively with 10% aqueous solution of NaOH, concentrated sulfuric acid and water, and dried over anhydrous sodium sulfate. After removing the solvent, the residue was crystallized from toluene to give 53.3 g of 3-cyano-2,4-dichloro-5-fluorobromobenzene (0.198 mol) in 86.2% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699992B2
Source datasetuspto-grants-2004_03
ORD IDord-f6ad75e6f33a41e3a3fc7e6b19cfe702
Source noteuspto-grants-2004_03