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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935407Generated: October 31, 2026

Benzoyl Peroxide → 4-Cyano-3-fluorobenzyl bromide

https://huagongshe.com/reaction/1935407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-4-methylbenzonitrileHCID 2778443—
SolventCarbon TetrachlorideHCID 5943—
Product4-Cyano-3-fluorobenzyl bromideHCID 2778466—

Reaction Steps

To a solution of the product from Step A (22.2 g, 165 mmol) in 220 mL of carbontetrachloride was added N-bromosuccinimide (29.2 g, 164 mmol) and benzoylperoxide (1.1 g). The reaction was heated to reflux for 30 minutes, then cooled to room temperature. The solution was concentrated in vacuo to one-third the original volume, poured into EtOAc, washed with water, sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. Analysis by 1H NMR indicated only partial conversion, so the crude material was resubjected to the same reaction conditions for 2.5 hours, using 18 g (102 mmol) of N-bromosuccinimide. After workup, the crude material was purified by silica gel chromatography (0-10% EtOAc/hexane) to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387903B1
Source datasetuspto-grants-2002_05
ORD IDord-7dc71765fb1945ff92f5507dde82a28f
Source noteuspto-grants-2002_05