Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803738Generated: November 2, 2026

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

https://huagongshe.com/reaction/1803738

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 numberUS08350084B2
Source datasetuspto-grants-2013_01
ORD IDord-18229e0e17eb41c3b08b04867172ebbd
Source noteuspto-grants-2013_01