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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857695Generated: November 1, 2026

Azobisisobutyronitrile → 4-(2-Bromomethyl-phenyl)-[1,2,3]thiadiazole

https://huagongshe.com/reaction/857695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant4-o-Tolyl-[1,2,3]thiadiazoleHCID 11275338—
SolventChloroformHCID 6212—
Product4-(2-Bromomethyl-phenyl)-[1,2,3]thiadiazoleHCID 21866243—

Reaction Steps

A solution of 4-o-tolyl-[1,2,3]thiadiazole (100 mg, 0.57 mmol), N-bromosuccinimide (100 mg, 0.57 mmol) and 2,2′-azobisisobutyronitrile (9.4 mg, 0.057 mmol) in chloroform (10 ml) was heated at reflux temperature for ˜18 h. Additional chloroform was added and the mixture was washed with water, 5% sodium thiosulfate solution and brine. Drying and solvent evaporation gave 4-(2-bromomethyl-phenyl)-[1,2,3]thiadiazole; 1H NMR (CDCl3, 300 MHz) δ 8.87 (s, 1H), 7.67–7.39 (m, 4H), 4.71 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144899B2
Source datasetuspto-grants-2006_12
ORD IDord-2237a15e53734b268c87248113e90dd1
Source noteuspto-grants-2006_12