Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028549Generated: October 27, 2026

Azobisisobutyronitrile → 2-Bromo-5-chlorobenzyl bromide

https://huagongshe.com/reaction/1028549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-chlorotolueneHCID 84476—
SolventCarbon TetrachlorideHCID 5943—
SolventHexaneHCID 8058—
Product2-Bromo-5-chlorobenzyl bromideHCID 11846505—

Reaction Steps

A mixture of 2-bromo-5-chloro-toluene (2.00 g, 9.75 mmol), NBS (2.08 g, 11.7 mmol) and catalytic amount of AIBN in carbon tetrachloride (50 ml) was stirred under refluxing conditions for 4 h. TLC (EtOAc:hexane=5:95) showed no starting material. The mixture was filtered and the filtrate was concentrated. The title compound was obtained as a white solid after flash column using EtOAc:hexane=5:95 as the elute. 1H NMR (CDCl3, 500 MHz) δ 7.53 (d, J=9.0 Hz, 1H), 7.47 (d, J=2.5 Hz, 1H), 7.18 (dd, J=8.5, 2.5 Hz, 1H), 4.60 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735435B2
Source datasetuspto-grants-2014_05
ORD IDord-bcbd146cf9314629918d7a61ea1c23ce
Source noteuspto-grants-2014_05