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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666716Generated: October 30, 2026

N-bromobutanimide → 4-(Bromomethyl)-3-fluorobenzonitrile

https://huagongshe.com/reaction/1666716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Fluoro-4-methylbenzonitrileHCID 585140—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-3-fluorobenzonitrileHCID 278314911.1%

Reaction Steps

To a solution of 3-fluoro-4-methylbenzonitrile (5.0 g, 0.23 mol) in 100 mL of carbon tetrachloride was added N-bromosuccinimide (4.97 g, 0.28 mol) and AIBN (100 mg, 0.61 mmol) and the mixture was refluxed for six hours. The reaction was cooled and filtered. The filtrate was washed with water, dried over magnesium sulfate, filtered and the solvents were removed under vacuum to afford 5.44 g of the title compound as an off-white solid. 1H NMR indicated the presence of 20% starting material. 1H NMR (400 MHz, CDCl3) for the title compound: δ 7.54-7.30 (m, 3H), 4.83 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044077B2
Source datasetuspto-grants-2011_10
ORD IDord-9c907d735eee42fb9ba0dff75fb893f2
Source noteuspto-grants-2011_10