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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8102Erstellt: 24. Oktober 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/de/reaction/8102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktN-bromobutanimideHCID 67184—
Edukt3-Methylbenzo[b]thiopheneHCID 73817—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt3-(Bromomethyl)-1-benzothiopheneHCID 1126464142,2%

Reaktionsschritte

3-Methylbenzo[b]thiophene (9.9 g, 67 mmol) is heated in carbon tetrachloride (133 ml ) to near reflux in the presence of n-bromosuccinimide (11.9 g, 67 mmol, 1.0 eq.). 2,2′Azobisisobutyronitrile (2.2 g, 13.3 mmol, 0.2 eq.) is added and the resulting mixture is refluxed for two hours. After cooling, the reaction mixture is filtered through a glass-fritted funnel, and the filtrate is concentrated. The residue is triturated with petroleum ether and toluene to afford 6.42 g of 3-Bromomethylbenzo[b]thiophene (42%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087635B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-891086c3a8cc43c7beb58f68c0a282e1
Quellennotizuspto-grants-2006_08