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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | (NE)-N-[(4-bromo-2,5-difluorophenyl)methylidene]hydroxylamine | HCID 90310471 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-2,5-difluorobenzonitrile | HCID 14984912 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09113629B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-1e1a92b39dc64c6a9286b85c2c873bce |
|---|
| Source note | uspto-grants-2015_08 |
|---|