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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrate;hydrochloride | HCID 21885828 | — |
| Reactant | 3-Cyano-2,4-dichloro-5-fluoroaniline | HCID 23431778 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | 3-Cyano-2,4-dichloro-5-fluorobromobenzene | HCID 23431790 | 86.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699992B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-f6ad75e6f33a41e3a3fc7e6b19cfe702 |
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| Source note | uspto-grants-2004_03 |
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