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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1272222Erstellt: 26. Oktober 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/1272222

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
PatentnummerUS07208505B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-60dcc74147ce49ca9e0d702b0b0b53ad
Quellennotizuspto-grants-2007_04