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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278159Erstellt: 25. Oktober 2026

Benzoyl Peroxide → 4-Cyano-3-fluorobenzyl bromide

https://huagongshe.com/reaction/278159

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt2-Fluoro-4-methylbenzonitrileHCID 2778443—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt4-Cyano-3-fluorobenzyl bromideHCID 2778466—

Reaktionsschritte

To a solution of the product from Step C (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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358985B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-0820a53ea7a745d798d5c82f7b972f94
Quellennotizuspto-grants-2002_03