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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19256Erstellt: 24. Oktober 2026

Benzoyl Peroxide → (E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/de/reaction/19256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt(E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl esterHCID 66895334—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt(E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl esterHCID 6689374431,6%

Reaktionsschritte

To a stirred mixture of (E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester (5.80 g, 0.020 mol) in carbon tetrachloride (30 mL) under a nitrogen atmosphere was added N-bromosuccinimide (5.51 g, 0.031 mol) and benzoyl peroxide (500 mg, 0.002 mol). Nitrogen gas was bubbled through the mixture for 5 min, and the resulting mixture was heated to reflux for 4 h. The reaction mixture was then placed in the refrigerator overnight. The solids formed were removed by filtration and the filtrate concentrated in vacuo. The crude product obtained was purified using flash column chromatography (silica gel (100-200 mesh), ethyl acetate/hexanes) to afford (E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester (2.30 g, 31%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b7d634ae72814e9599086035e6f89c16
Quellennotizuspto-grants-2010_06