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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506604Generated: October 31, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1506604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-3-methylbenzonitrileHCID 23160359—
Solvent1,2-DichloroethaneHCID 11—
Product3-(Bromomethyl)-2-fluorobenzonitrileHCID 66678465—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 2-fluoro-3-methylbenzonitrile (200 mg, 1.5 mmol) in 1,2-dichloroethane (30 ml) was added NBS (266 mg, 1.49 mmol) and AIBN (29 mg, 0.15 mmol) at RT. The reaction mixture was then heated to 80° C., and the reaction mixture was stirred for 2 h. After complete consumption of the starting material (by TLC), the reaction mixture was cooled to RT. The volatiles were removed under reduced pressure to obtain the crude material. Purification by silica gel column chromatography eluting with 2-3% EtOAc/hexane afforded compound I-6 (250 mg, 1.15 mmol, 78%) as colorless liquid. 1H NMR (500 MHz, CDCl3): δ 7.69-7.65 (m, 1H), 7.62-7.58 (m, 1H), 7.28-7.25 (m, 1H), 4.50 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09220265B2
Source datasetuspto-grants-2015_12
ORD IDord-5469a139b2514361bd7806aaf30946d6
Source noteuspto-grants-2015_12