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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19217Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/19217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt(E)-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl esterHCID 67504254—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt(E)-4-bromo-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl esterHCID 6750452251,3%

Reaktionsschritte

To a stirred mixture of (E)-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester (3.20 g, 0.012 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (3.26 g, 0.018 mol) and benzoyl peroxide (295 mg, 0.001 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-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester (2.10 g, 50%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-bb3f25397f944f85a7a90471a6a73096
Quellennotizuspto-grants-2010_06