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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8102Generated: October 25, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/8102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Methylbenzo[b]thiopheneHCID 73817—
SolventCarbon TetrachlorideHCID 5943—
Product3-(Bromomethyl)-1-benzothiopheneHCID 1126464142.2%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087635B2
Source datasetuspto-grants-2006_08
ORD IDord-891086c3a8cc43c7beb58f68c0a282e1
Source noteuspto-grants-2006_08