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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279774Generated: October 30, 2026

Azobisisobutyronitrile → 4-(Bromomethyl)-2-chloro-1-nitrobenzene

https://huagongshe.com/reaction/2279774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Chloro-4-nitrotolueneHCID 123478—
Solvent(Trifluoromethyl)benzeneHCID 7368—
Product4-(Bromomethyl)-2-chloro-1-nitrobenzeneHCID 67193371—

Reaction Steps

A solution of 3-chloro-4-nitrotoluene (2.0 g, 12 mmol), NBS (2.62 g, 14.6 mmol) and 2,2′-azo-bis-isobutyronitrile (0.195 g, 1.16 mmol) in α,α,α-trifluorotoluene (200 mL) was heated at 80° C. under an atmosphere of nitrogen for 3 h. Solvent was removed in vacuo and the residue was partitioned between EtOAc and water and separated. The aqueous layer was extracted with EtOAc (3×) and the combined organic fractions were washed with brine, dried over sodium sulfate, filtered, and concentrated. The crude product was taken to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133224B2
Source datasetuspto-grants-2015_09
ORD IDord-4746a1d597b740af9e5f49161fd261f4
Source noteuspto-grants-2015_09