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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058330Generated: October 27, 2026

Azobisisobutyronitrile → [2-(Bromomethyl)phenyl]acetic acid

https://huagongshe.com/reaction/1058330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactanto-Tolylacetic acidHCID 69519—
SolventCarbon TetrachlorideHCID 5943—
Product[2-(Bromomethyl)phenyl]acetic acidHCID 12889260—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of 97.0 g (0.646 mol) o-tolylacetic acid in 1.75 L carbon tetrachloride was added 115.0 g (0.646 mol) N-bromosuccinimide and 3.4 g (0.021 mol) 2,2′-azobisisobutyronitrile. The mixture was heated at reflux under a nitrogen atmosphere for 4 h. After the mixture was cooled to 0-5° C. for 30 min, the solids were removed by filtration and washed with a small portion of carbon tetrachloride. This solid was triturated with water (0.8 L), collected on a filter, and washed with 500 mL of water to give 2-bromomethylphenylacetic acid. The filtrate was concentrated to a volume of 150 ml, and the resulting slurry cooled to 0-5° C. for 30 min. A second batch of product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515011B2
Source datasetuspto-grants-2003_02
ORD IDord-32516d67db21493ca0b55eeba5422a1f
Source noteuspto-grants-2003_02