Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604683Generated: October 29, 2026

Azobisisobutyronitrile → 5-Bromo-4-(bromomethyl)-2-phenyl-1,3-thiazole

https://huagongshe.com/reaction/604683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Bromo-4-methyl-2-phenyl-1,3-thiazoleHCID 2795494—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromo-4-(bromomethyl)-2-phenyl-1,3-thiazoleHCID 67057757—

Reaction Steps

A mixture of 5-Bromo-4-methyl-2-phenyl-1,3-thiazole (1.00 g, 3.93 mmol), NBS (0.84 g, 4.72 mmol) and catalytic amount of AIBN in CCl4 (20 mL) was heated at reflux for 24 h. No starting material was seen by 1H NMR. The solvent was removed. The title compound was obtained as a colorless solid after flash chromatography using EtOAc/hexane (3:97) as the eluant. 1H NMR (500 MHz, CDCl3): δ 7.90 (m, 3H), 7.48 (m, 2H), 4.61 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-466915342bb04b1bb10b725b02990c3b
Source noteuspto-grants-2011_03