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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516549Generated: October 29, 2026

Cyanuric chloride → 4-Bromo-2,5-difluorobenzonitrile

https://huagongshe.com/reaction/516549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant(NE)-N-[(4-bromo-2,5-difluorophenyl)methylidene]hydroxylamineHCID 90310471—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2,5-difluorobenzonitrileHCID 1498491268%

Reaction Steps

A solution of cyanuric chloride (3.12 g, 16.94 mmol) and dry DMF (8.5 mL) was stirred for 30 min or until the formation of white solid. Disappearance of cyanuric chloride was confirmed by TLC. (E)-4-bromo-2,5-difluorobenzaldehyde oxime (4.0 g, 16.94 mmol) in DMF (26 mL) was added dropwise to the suspension and stirred for 1 h. The reaction mixture was diluted with water and extracted with hexanes. The organic extract was washed with water, washed with saturated brine solution, dried (Na2SO4), filtered, and evaporated to dryness under reduced pressure. The crude product was purified by flash chromatography (SiO2, eluting with 2-20% ethyl acetate in hexanes) to provide the title compound as a white solid (2.5 g, 68%): 1H NMR (400 MHz, CDCl3) δ 7.40 (dd, J=5.36, 7.10 Hz, 1H), 7.52 (dd, J=5.40, 7.66 Hz, 1H); EIMS m/z 218.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-1e1a92b39dc64c6a9286b85c2c873bce
Source noteuspto-grants-2015_08