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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351434Erstellt: 25. Oktober 2026

{1-[4-(Benzyloxy)phenyl]ethenyl}(tributyl)stannane → 2,3-Di(4-benzyloxy-phenyl)-1,3-butadiene

https://huagongshe.com/reaction/351434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt{1-[4-(Benzyloxy)phenyl]ethenyl}(tributyl)stannaneHCID 18436367—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2,3-Di(4-benzyloxy-phenyl)-1,3-butadieneHCID 18436331—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a cooled solution of tributyl-[1-(4-benzyloxy-phenyl)-vinyl]-stannane (26.2 g, 52.6 mmol) in DMF (180 mL) at 0° C. was added CuCl (8.6 g, 87.7 mmol) and CuCl2 (1.00 g, 8.13 mmol), which was then stirred at 25° C. for 2 h. The reaction mixture was then diluted with ethyl acetate (500 mL) and washed with brine (3×300 mL). The reaction mixture was then dried over MgSO4 and purified by SiO2 (20% ethyl acetate/hexane) to yield 2,3-di(4-benzyloxy-phenyl)-1,3-butadiene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183445B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-7d8fd34e7b16494ab4b6b84115eb2720
Quellennotizuspto-grants-2007_02