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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272222Generated: October 26, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/1272222

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 numberUS07208505B2
Source datasetuspto-grants-2007_04
ORD IDord-60dcc74147ce49ca9e0d702b0b0b53ad
Source noteuspto-grants-2007_04