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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7732Erstellt: 23. Oktober 2026

Benzoyl Peroxide → 2-[4-(Bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole

https://huagongshe.com/de/reaction/7732

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt2-(3-Methoxy-4-methylphenyl)-1,3-benzoxazoleHCID 21990968—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt2-[4-(Bromomethyl)-3-methoxyphenyl]-1,3-benzoxazoleHCID 21990991—

Reaktionsschritte

2-(3-Methoxy-4-methylphenyl)-1,3-benzoxazole (1.0 g, 4.1 mmol), carbon tetrachloride (18 mL), benzoyl peroxide (66 mg, 0.3 mmol) and N-bromosuccinimide (970 mg, 5.4 mmol) was heated to reflux conditions under argon and placed under a UV light. After 1 h, no starting material was observed by TLC. After cooling mixture to rt, filtered, washing with dichoromethane. After concentrating filtrate in vacuo, the resulting colorless solid was purified by flash chromatography, using a gradient elution of 1:4 EtOAc:hexanes to EtOAc. This afforded the desired intermediate, 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole, as a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087601B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-7b5dc4ac04c6402099cfcfbd4e02fa1a
Quellennotizuspto-grants-2006_08