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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572549Generated: October 29, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-5-fluorobenzonitrile

https://huagongshe.com/reaction/572549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Fluoro-5-methylbenzonitrileHCID 2778446—
SolventAcetonitrileHCID 6342—
Product3-(Bromomethyl)-5-fluorobenzonitrileHCID 66652629—

Reaction Conditions

Temperature70 °C

Reaction Steps

3-Fluoro-5-methylbenzonitrile (Hognda Trading; 100 g, 0.74 mol) was taken in acetonitrile (1 L) at 25° C. under nitrogen atmosphere. N-Bromosuccinimide (105 g, 0.59 mol) and AIBN (2.4 g, 0.014 mol) were added and the reaction mixture was heated at 70° C. for 1 h 20 minutes. The reaction mixture was cooled to 25° C. and concentrated. The residue was diluted, cooled to 0-5° C. and stirred for 15 minutes at the same temperature. The precipitated succinimide was filtered and the filtrate was concentrated to get crude product as yellow oil (90 g). It was taken in petroleum ether (200 mL) and cooled to −20° C. stirred for 30 minutes. The precipitated solids were filtered and dried to get the title product as white solid. 1H NMR (DMSO-d6; 400 MHz): δ 7.83 (m, 2H), 7.73 (m, 1H), 4.72 (s, 2H). HPLC (Method A) Rt: 4.17 min (Purity: 99.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029405B2
Source datasetuspto-grants-2015_05
ORD IDord-f45ca2caf7854056af437cc9a310816c
Source noteuspto-grants-2015_05