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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400257Generated: November 3, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/2400257

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 numberUS08796001B2
Source datasetuspto-grants-2014_08
ORD IDord-e161c0751dcc4d6ab09491ac4725617b
Source noteuspto-grants-2014_08