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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19275Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/19275

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt(E)-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl esterHCID 66895231—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt(E)-4-bromo-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl esterHCID 6689459856,6%

Reaktionsschritte

To a stirred mixture of (E)-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester (5.33 g, 0.019 mol) in carbon tetrachloride (30 mL) under a nitrogen atmosphere was added N-bromosuccinimide (5.20 g, 0.029 mol) and benzoyl peroxide (470 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-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester (3.80 g, 55%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-89b830132c7d4d35857e2545e6a12ca4
Quellennotizuspto-grants-2010_06