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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1711084Erstellt: 25. Oktober 2026

Azobisisobutyronitrile → 1-(Bromomethyl)-4-fluoro-2-iodobenzene

https://huagongshe.com/reaction/1711084

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktN-bromobutanimideHCID 67184—
Edukt4-Fluoro-2-iodotolueneHCID 83220—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt1-(Bromomethyl)-4-fluoro-2-iodobenzeneHCID 1280605458%

Reaktionsschritte

N-Bromosuccinimide (0.61 g, 3.4 mmol) and VAZO (0.10 g, 0.41 mmol) were added to a solution of 4-fluoro-2-iodotoluene (0.75 g, 3.2 mmol) in carbon tetrachloride (45 mL). The resulting suspension was stirred and heated under reflux for 18 hours. It was then cooled and filtered, the solid was rinsed with carbon tetrachloride (5 mL), and the combined filtrates were concentrated under reduced pressure. The residue was purified by flash column chromatography (eluting with hexanes) to provide 322 (0.58 g, 58% yield). 1H NMR (400 MHz, CDCl3) δ (ppm): 7.51 (dd, J=8.0, 2.5 Hz, 1H); 7.38 (dd, J=8.4, 5.7 Hz, 1H); 7.00 (dt, J=8.2, 2.7 Hz, 1H); 4.54 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790729B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-2330a2641b644ba894609481f9315db2
Quellennotizuspto-grants-2010_09