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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29246Erstellt: 23. Oktober 2026

Azobisisobutyronitrile → (6-Bromo-3-bromomethyl-benzofuran-2-yl)(2,4-dichlorophenyl)-methanone

https://huagongshe.com/de/reaction/29246

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktN-bromobutanimideHCID 67184—
Edukt(6-Bromo-3-methyl-benzofuran-2-yl)(2,4-dichloro-phenyl)methanoneHCID 59788907—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt(6-Bromo-3-bromomethyl-benzofuran-2-yl)(2,4-dichlorophenyl)-methanoneHCID 5978888878,9%

Reaktionsschritte

To a solution of (6-bromo-3-methyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone (3.0 g, 7.81 mmol) in carbon tetrachloride (30 mL) was added N-bromosuccinimide (1.46 g, 8.2 mmol) and 2,2′-azobisisobutyronitrile (128 mg, 0.78 mmol). The reaction mixture was refluxed for 6 h, then filtered. The filtrate was concentrated and the crude product was triturated with 10% EtOAc/hexane to afford the desired product as a pale yellow solid (2.85 g, 78.9%). This material was used in the subsequent step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420066B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-e72283bc9ddc4e078eb8f910a1eef417
Quellennotizuspto-grants-2008_09