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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427908Generated: November 2, 2026

Azobisisobutyronitrile → 4-(bromomethyl)-5-chloro-2-fluoro-N-(methylsulfonyl)benzamide

https://huagongshe.com/reaction/1427908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Chloro-2-fluoro-4-methyl-N-(methylsulfonyl)benzamideHCID 58042368—
Solvent1,2-DichloroethaneHCID 11—
Product4-(bromomethyl)-5-chloro-2-fluoro-N-(methylsulfonyl)benzamideHCID 58042397—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-chloro-2-fluoro-4-methyl-N-(methylsulfonyl)benzamide (0.8 g, 3.0 mmol), N-bromosuccinimide (1.6 g, 9.0 mmol) and azodiisobutyronitrile (16 mg, 0.09 mmol) in 1,2-dichloroethane (20 mL) was stirred at 90° C. for 16 hrs. The reaction was quenched with Na2S2O3 (10 mL, 10%), extracted with 1,2-dichloroethane (20 mL×3), dried over anhydrous Na2SO4, concentrated and the residue was used in next step without further purification (1.1 g, crude). LCMS (ESI) m/z: 342.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933236B2
Source datasetuspto-grants-2015_01
ORD IDord-4dfbde27ee814d9286f78d95ecb4ef28
Source noteuspto-grants-2015_01